A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638896



Internal ID7025681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67996500..68001705hg38UCSC Ensembl
Innerchr16:67996500..68001705hg38UCSC Ensembl
Outerchr16:67996374..68001841hg38UCSC Ensembl
chr16:68030403..68035608hg19UCSC Ensembl
Innerchr16:68030403..68035608hg19UCSC Ensembl
Outerchr16:68030277..68035744hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385206
hg195206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501605
SamplesHG00536
Known GenesDPEP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638896
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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