A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959134



Internal ID16253090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13029299..13089801hg38UCSC Ensembl
Innerchr3:13070799..13131301hg19UCSC Ensembl
Innerchr3:13045799..13106301hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3860503
hg1960503
hg1860503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589722
Supporting Variants
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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