A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582964



Internal ID18881245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:150679272..150886008hg38UCSC Ensembl
Innerchr2:151535786..151742522hg19UCSC Ensembl
Innerchr2:151244032..151450768hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38206737
hg19206737
hg18206737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010993
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)nssv3582964
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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