A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15498506



Internal ID1433538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63492203..63581783hg38UCSC Ensembl
Innerchr16:63492232..63581754hg38UCSC Ensembl
Outerchr16:63492174..63581812hg38UCSC Ensembl
chr16:63526107..63615687hg19UCSC Ensembl
Innerchr16:63526136..63615658hg19UCSC Ensembl
Outerchr16:63526078..63615716hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3889581
hg1989581
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638816
Supporting Variants
SamplesHG01312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15498506
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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