A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083559



Internal ID15936745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44955728..44962092hg38UCSC Ensembl
Innerchr7:44995327..45001691hg19UCSC Ensembl
Innerchr7:44961852..44968216hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg386365
hg196365
hg186365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606809
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)nssv1083559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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