A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010266



Internal ID19099484
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 StatusM
Merged Variants
Supporting Variantsnssv3577290
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)nsv1010266
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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