A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079659



Internal ID15932845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20696954..20711226hg38UCSC Ensembl
Innerchr7:20736577..20750849hg19UCSC Ensembl
Innerchr7:20703102..20717374hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3814273
hg1914273
hg1814273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606371
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)nssv1079659
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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