A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12437955



Internal ID6009680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77155374..77166040hg38UCSC Ensembl
Innerchr6:77155375..77166040hg38UCSC Ensembl
Outerchr6:77155374..77166041hg38UCSC Ensembl
chr6:77865091..77875757hg19UCSC Ensembl
Innerchr6:77865092..77875757hg19UCSC Ensembl
Outerchr6:77865091..77875758hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810667
hg1910667
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609626
Supporting Variants
SamplesNA19404
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12437955
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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