A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583982



Internal ID18535577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:195637334..195666943hg38UCSC Ensembl
Innerchr2:196502058..196531667hg19UCSC Ensembl
Innerchr2:196210303..196239912hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3829610
hg1929610
hg1829610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999936
Supporting Variants
Samples
Known GenesSLC39A10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583982
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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