A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962601



Internal ID15909871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46769856..46808731hg38UCSC Ensembl
Innerchr3:46811346..46850221hg19UCSC Ensembl
Innerchr3:46786350..46825225hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3838876
hg1938876
hg1838876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590203
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)nssv962601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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