A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12461657



Internal ID5990660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91123322..91158201hg38UCSC Ensembl
Innerchr6:91123322..91158201hg38UCSC Ensembl
Outerchr6:91122822..91158701hg38UCSC Ensembl
chr6:91833040..91867919hg19UCSC Ensembl
Innerchr6:91833040..91867919hg19UCSC Ensembl
Outerchr6:91832540..91868419hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3834880
hg1934880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609934
Supporting Variants
SamplesNA19394
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12461657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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