A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610990



Internal ID6997905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140076385..140188736hg38UCSC Ensembl
Innerchr6:140076395..140188727hg38UCSC Ensembl
Outerchr6:140076376..140188746hg38UCSC Ensembl
chr6:140397522..140509873hg19UCSC Ensembl
Innerchr6:140397532..140509864hg19UCSC Ensembl
Outerchr6:140397513..140509883hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38112352
hg19112352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12567987, essv12567986, essv12567988
SamplesNA20296, HG01817, HG02778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610990
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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