A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496286



Internal ID4709578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61616576..61632925hg38UCSC Ensembl
Innerchr16:61616626..61632875hg38UCSC Ensembl
Outerchr16:61616516..61632985hg38UCSC Ensembl
chr16:61650480..61666829hg19UCSC Ensembl
Innerchr16:61650530..61666779hg19UCSC Ensembl
Outerchr16:61650420..61666889hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3816350
hg1916350
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638780
Supporting Variants
SamplesHG04229
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496286
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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