A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010262



Internal ID19099480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:8517172..8551709hg38UCSC Ensembl
Innerchr2:8657302..8691839hg19UCSC Ensembl
Innerchr2:8574753..8609290hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3834538
hg1934538
hg1834538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3713n100
Supporting Variantsnssv3576945
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)nsv1010262
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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