A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006641



Internal ID19095858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33478025..33527699hg38UCSC Ensembl
Innerchr3:33519517..33569191hg19UCSC Ensembl
Innerchr3:33494521..33544195hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3849675
hg1949675
hg1849675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739672
Samples
Known GenesCLASP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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