A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666491



Internal ID9585910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149073524..149079630hg38UCSC Ensembl
Outerchr7:149073153..149080000hg38UCSC Ensembl
Innerchr7:148770616..148776722hg19UCSC Ensembl
Outerchr7:148770245..148777092hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386848
hg196848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6424619, essv6166645, essv6161217, essv5957425, essv6377708, essv6474965, essv5588694, essv6593726, essv5737517, essv5993868, essv5862010, essv5668050, essv6089254, essv6185703, essv6573461, essv6012965, essv5884605, essv6022847, essv6465389, essv5613846, essv5988489, essv6060355, essv5620702, essv5766009, essv6010387, essv5815298, essv6463462, essv6514933, essv5528712, essv5505266, essv5443033, essv5425439, essv5423523, essv6035780, essv5845093
SamplesHG00403, HG00542, HG00442, HG00536, HG00524, HG00699, HG00654, HG00702, HG00689, HG00634, HG00610, HG00537, HG00590, HG00683, HG00534, HG00427, HG00530, HG00464, HG00629, HG00443, HG00428, HG00653, HG00701, HG00500, HG00619, HG00690, HG00684, HG00613, HG00525, HG00704, HG00476, HG00473, HG00607, HG00620, HG00478
Known GenesZNF786
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666491
Frequency
Sample Size1151
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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