A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609623



Internal ID6996544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76862822..76869544hg38UCSC Ensembl
Innerchr6:76862822..76869544hg38UCSC Ensembl
Outerchr6:76862322..76870044hg38UCSC Ensembl
chr6:77572539..77579261hg19UCSC Ensembl
Innerchr6:77572539..77579261hg19UCSC Ensembl
Outerchr6:77572039..77579761hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386723
hg196723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12437899, essv12437898
SamplesNA20346, NA20340
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609623
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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