A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957818



Internal ID15905088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:972724..1028355hg38UCSC Ensembl
Innerchr3:1014408..1070039hg19UCSC Ensembl
Innerchr3:989408..1045039hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3855632
hg1955632
hg1855632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589310
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)nssv957818
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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