A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079661



Internal ID15932847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20704920..20715352hg38UCSC Ensembl
Innerchr7:20744543..20754975hg19UCSC Ensembl
Innerchr7:20711068..20721500hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3810433
hg1910433
hg1810433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606373
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)nssv1079661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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