A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15563490



Internal ID4091860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88291388..88293411hg38UCSC Ensembl
Innerchr16:88291394..88293406hg38UCSC Ensembl
Outerchr16:88291383..88293417hg38UCSC Ensembl
chr16:88324994..88327017hg19UCSC Ensembl
Innerchr16:88325000..88327012hg19UCSC Ensembl
Outerchr16:88324989..88327023hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382024
hg192024
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639545
Supporting Variants
SamplesHG03717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15563490
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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