A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020434



Internal ID19109653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46151717..46334765hg38UCSC Ensembl
Innerchr5:46151819..46334867hg19UCSC Ensembl
Innerchr5:46187576..46370624hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38183049
hg19183049
hg18183049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5646n100
Supporting Variantsnssv3637970
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)nsv1020434
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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