A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610257



Internal ID6997174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105732428..105739290hg38UCSC Ensembl
Innerchr6:105732428..105739290hg38UCSC Ensembl
Outerchr6:105732237..105739392hg38UCSC Ensembl
chr6:106180303..106187165hg19UCSC Ensembl
Innerchr6:106180303..106187165hg19UCSC Ensembl
Outerchr6:106180112..106187267hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386863
hg196863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12496946
SamplesNA20851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610257
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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