A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613692



Internal ID7000588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73914894..73916918hg38UCSC Ensembl
Innerchr7:73914894..73916918hg38UCSC Ensembl
Outerchr7:73914558..73917202hg38UCSC Ensembl
chr7:73329224..73331248hg19UCSC Ensembl
Innerchr7:73329224..73331248hg19UCSC Ensembl
Outerchr7:73328888..73331532hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12841062, essv12841070, essv12841066, essv12841064, essv12841065, essv12841067, essv12841068, essv12841063, essv12841069, essv12841060, essv12841061, essv12841059
SamplesHG02385, NA20508, HG02122, NA20532, NA18595, HG02178, HG02134, HG03858, NA20801, HG01375, NA21102, HG01618
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613692
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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