A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083569



Internal ID15936755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44960264..44961927hg38UCSC Ensembl
Innerchr7:44999863..45001526hg19UCSC Ensembl
Innerchr7:44966388..44968051hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381664
hg191664
hg181664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606817
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)nssv1083569
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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