A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609500



Internal ID6996421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73211589..73212239hg38UCSC Ensembl
Innerchr6:73211646..73212182hg38UCSC Ensembl
Outerchr6:73211532..73212296hg38UCSC Ensembl
chr6:73921312..73921962hg19UCSC Ensembl
Innerchr6:73921369..73921905hg19UCSC Ensembl
Outerchr6:73921255..73922019hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12419409
SamplesNA18547
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609500
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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