A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662160



Internal ID9928265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73487066..73487330hg38UCSC Ensembl
Outerchr14:73487029..73487380hg38UCSC Ensembl
Innerchr14:73953771..73954035hg19UCSC Ensembl
Outerchr14:73953734..73954085hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv400e199
Supporting Variantsessv5682409, essv5868664, essv5651672, essv5546635, essv5685363, essv6512754, essv5774891, essv6001063, essv5915201, essv6383283, essv6388054, essv5621130, essv5425141, essv6020622, essv6378167, essv6472464, essv5572442, essv6200413, essv6036968, essv5652309, essv6207552, essv6146150, essv5803694, essv6274753, essv6381552, essv5759623, essv6055450, essv6109715, essv6582563, essv5824923, essv6333483, essv6302008, essv6274455, essv6492650, essv5568177, essv6401153, essv6260803, essv5628331, essv5958928, essv5736195, essv5459995, essv5604429, essv5444294, essv6119855, essv5535206, essv5552946, essv5790423, essv6457339, essv5797492, essv5506468, essv5847746, essv6390836, essv6244589, essv6209558, essv5688088, essv5563468, essv6258193, essv6548993, essv6402221, essv5955273, essv5874542, essv6070385, essv5748088, essv5423750, essv6557156, essv6176544, essv6109388, essv6305144, essv6111284, essv5785374, essv5582126, essv6064050, essv6439158, essv6299554, essv6418475, essv6257455, essv5770975, essv6597007, essv5728106, essv6378249, essv5527432, essv5820916, essv5861581, essv6003950, essv6512149, essv5767880, essv5639138, essv5840022, essv5871292, essv5811465
SamplesHG00626, HG00650, HG01356, HG00536, NA19397, HG00608, HG00671, NA18980, HG01066, NA18999, NA19393, NA18526, HG01051, HG00261, HG00693, HG00663, NA19396, NA19076, NA19379, NA18944, HG00589, HG00501, HG00702, HG00689, HG00448, NA18635, NA20756, NA18567, NA18558, NA18574, NA12283, HG01083, HG00334, NA20513, HG00537, NA19130, HG00590, NA12282, HG00683, HG01170, NA18977, NA18560, NA18990, NA18557, NA18985, HG00419, HG00253, NA19007, NA18544, NA18613, HG00443, HG00475, HG00556, HG00583, NA18534, HG00708, HG01390, HG00613, HG00321, NA12827, HG00704, NA18536, HG01075, NA20765, NA18608, NA19375, NA18632, HG00580, NA07051, HG01357, HG00473, HG00418, HG00620, NA19376, HG00707, HG00672, HG00259, HG00656, HG00342, HG00698, NA18552, HG01377, HG00472, NA18624, NA18549, HG00437, NA18562, HG00581, NA18577, NA18620
Known GenesHEATR4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662160
Frequency
Sample Size1151
Observed Gain0
Observed Loss90
Observed Complex0
Frequencyn/a


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