A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020158



Internal ID19109377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121037623..121248357hg38UCSC Ensembl
Innerchr5:120373318..120584052hg19UCSC Ensembl
Innerchr5:120401217..120611951hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38210735
hg19210735
hg18210735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5804n100
Supporting Variantsnssv3648034
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)nsv1020158
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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