A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998067



Internal ID19157604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20150990..20186578hg38UCSC Ensembl
Innerchr2:20350751..20386339hg19UCSC Ensembl
Innerchr2:20214232..20249820hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3835589
hg1935589
hg1835589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3739n100
Supporting Variantsnssv3578997, nssv3578998
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)nsv998067
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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