A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963063



Internal ID16257019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52055821..52056677hg38UCSC Ensembl
Innerchr3:52089837..52090693hg19UCSC Ensembl
Innerchr3:52064877..52065733hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38857
hg19857
hg18857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590283
Supporting Variants
Samples
Known GenesDUSP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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