A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019323



Internal ID19108541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46136718..46313527hg38UCSC Ensembl
Innerchr5:46136820..46313629hg19UCSC Ensembl
Innerchr5:46172577..46349386hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38176810
hg19176810
hg18176810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5646n100
Supporting Variantsnssv3637950
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)nsv1019323
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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