A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675938



Internal ID9595357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3528789..3528834hg38UCSC Ensembl
Outerchr19:3528632..3528987hg38UCSC Ensembl
Innerchr19:3528787..3528832hg19UCSC Ensembl
Outerchr19:3528630..3528985hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5971020, essv6167942, essv6585506, essv6409710, essv5644308, essv6442474, essv5812117, essv5679506, essv5572621, essv6096490, essv6334256, essv5752969, essv5461114, essv5485619, essv6484936, essv5439286, essv6589285, essv6346272, essv6260378, essv5766442, essv6116322, essv5556776, essv6265100, essv6066489, essv6001403, essv6571326, essv5444582, essv6044328, essv5499629, essv6504253, essv6102333, essv6457215, essv6306087, essv5399741, essv5997153, essv6124364, essv6264466, essv6378129, essv5684982, essv5414221, essv6448102, essv6256198, essv5701077, essv5761249, essv5968797, essv5614867
SamplesHG01441, NA07037, NA20527, HG01052, HG01075, NA19114, HG01173, NA19401, NA20299, NA19359, NA19451, NA18517, HG00375, HG01171, HG01521, HG00256, HG00158, NA20356, HG00140, NA19197, HG00231, HG01124, HG00330, NA19398, NA19380, HG01437, NA19395, NA19372, NA19384, NA18510, HG00282, HG00740, HG01383, NA20525, NA20276, HG01112, NA19399, NA19371, HG01125, NA19756, HG00251, HG00275, HG00324, HG01377, NA18519, NA07000
Known GenesFZR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675938
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer