A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079658



Internal ID15932844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20664325..20701544hg38UCSC Ensembl
Innerchr7:20703948..20741167hg19UCSC Ensembl
Innerchr7:20670473..20707692hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3837220
hg1937220
hg1837220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606370
Supporting Variants
Samples
Known GenesABCB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079658
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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