A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579356



Internal ID16366765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34481581..34482663hg38UCSC Ensembl
Innerchr19:34972486..34973568hg19UCSC Ensembl
Innerchr19:39664326..39665408hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381083
hg191083
hg181083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6409n54
Supporting Variantsnssv898593, nssv898594
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579356
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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