A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638735



Internal ID7025520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58933846..58941373hg38UCSC Ensembl
Innerchr16:58933846..58941373hg38UCSC Ensembl
Outerchr16:58933572..58941597hg38UCSC Ensembl
chr16:58967750..58975277hg19UCSC Ensembl
Innerchr16:58967750..58975277hg19UCSC Ensembl
Outerchr16:58967476..58975501hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387528
hg197528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15489800, essv15489799, essv15489801, essv15489802
SamplesHG00306, NA18560, HG00584, NA18549
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638735
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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