A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579276



Internal ID16366685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29566638..29567671hg38UCSC Ensembl
Innerchr19:30057545..30058578hg19UCSC Ensembl
Innerchr19:34749385..34750418hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381034
hg191034
hg181034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6394n54
Supporting Variantsnssv897579, nssv897578
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579276
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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