A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577290



Internal ID18875571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71291516..71355178hg38UCSC Ensembl
Innerchr2:71518646..71582308hg19UCSC Ensembl
Innerchr2:71372154..71435816hg18UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3863663
hg1963663
hg1863663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010266
Supporting Variants
Samples
Known GenesZNF638
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577290
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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