A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582992



Internal ID18881273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:160895010..161029592hg38UCSC Ensembl
Innerchr2:161751521..161886103hg19UCSC Ensembl
Innerchr2:161459767..161594349hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38134583
hg19134583
hg18134583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006835
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582992
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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