A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997958



Internal ID19157495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20149582..20186578hg38UCSC Ensembl
Innerchr2:20349343..20386339hg19UCSC Ensembl
Innerchr2:20212824..20249820hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3836997
hg1936997
hg1836997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3739n100
Supporting Variantsnssv3578994
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)nsv997958
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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