A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962606



Internal ID15909876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46832467..46894037hg38UCSC Ensembl
Innerchr3:46873957..46935527hg19UCSC Ensembl
Innerchr3:46848961..46910531hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3861571
hg1961571
hg1861571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590206
Supporting Variants
Samples
Known GenesMYL3, PRSS42, PTH1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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