A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3727692



Internal ID19025973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52527318..52581552hg38UCSC Ensembl
Innerchr2:52754456..52808690hg19UCSC Ensembl
Innerchr2:52607960..52662194hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3854235
hg1954235
hg1854235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010707
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)nssv3727692
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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