A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16314914



Internal ID3578621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34732206..34742608hg38UCSC Ensembl
Innerchr21:34732206..34742608hg38UCSC Ensembl
Outerchr21:34732023..34742912hg38UCSC Ensembl
chr21:36104504..36114905hg19UCSC Ensembl
Innerchr21:36104504..36114905hg19UCSC Ensembl
Outerchr21:36104321..36115209hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3810403
hg1910402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646927
Supporting Variants
SamplesHG03166
Known GenesLINC00160
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16314914
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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