A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079219



Internal ID15932405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13064011..13084531hg38UCSC Ensembl
Innerchr7:13103636..13124156hg19UCSC Ensembl
Innerchr7:13070161..13090681hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3820521
hg1920521
hg1820521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606247
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079219
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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