A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12608427



Internal ID4665696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159644889..159652771hg38UCSC Ensembl
Innerchr6:159645389..159652271hg38UCSC Ensembl
Outerchr6:159643889..159653771hg38UCSC Ensembl
chr6:160065921..160073803hg19UCSC Ensembl
Innerchr6:160066421..160073303hg19UCSC Ensembl
Outerchr6:160064921..160074803hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg387883
hg197883
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611420
Supporting Variants
SamplesHG04194
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12608427
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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