A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12453997



Internal ID3744380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83431767..83442564hg38UCSC Ensembl
Innerchr6:83431803..83442529hg38UCSC Ensembl
Outerchr6:83431732..83442600hg38UCSC Ensembl
chr6:84141486..84152283hg19UCSC Ensembl
Innerchr6:84141522..84152248hg19UCSC Ensembl
Outerchr6:84141451..84152319hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3810798
hg1910798
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609778
Supporting Variants
SamplesHG03376
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12453997
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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