A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668853



Internal ID9934958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11486143..11486334hg38UCSC Ensembl
chr16:11579999..11580190hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6457489, essv6449493, essv6218821, essv6297554, essv5511674, essv6363050, essv5893685, essv6345343, essv6204143, essv6341442, essv6352524, essv6508132, essv6506097, essv5935277, essv6059844, essv6471119, essv6041236, essv5439155, essv5847217, essv6331617, essv6112845, essv5989271, essv6092077, essv6411868, essv6598451, essv5546111, essv6230801, essv5535337, essv6344601, essv5534163, essv5932261, essv6460726, essv6120054, essv6354176, essv6442916, essv5996336, essv6038634
SamplesHG00442, HG00536, HG00671, NA18599, HG00449, HG00693, HG00271, HG00663, NA18550, NA18571, HG00590, NA18611, NA19404, HG00512, HG00534, HG00427, NA18557, HG00260, NA18637, NA18534, HG00284, NA18573, HG00651, HG01101, HG00525, HG00476, NA18559, HG00513, NA19093, NA18636, NA19116, NA18552, NA18623, NA18549, NA18622, HG01061, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668853
Frequency
Sample Size1151
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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