A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586963



Internal ID18885244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:238911116..238943769hg38UCSC Ensembl
Innerchr2:239832812..239865465hg19UCSC Ensembl
Innerchr2:239497749..239530402hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3832654
hg1932654
hg1832654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001361
Supporting Variants
Samples
Known GenesFLJ43879
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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