A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999642



Internal ID19159178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33457884..33521772hg38UCSC Ensembl
Innerchr3:33499376..33563264hg19UCSC Ensembl
Innerchr3:33474380..33538268hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3863889
hg1963889
hg1863889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589589
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)nsv999642
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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