A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579721



Internal ID16367130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43141405hg38UCSC Ensembl
Innerchr19:43374601..43645557hg19UCSC Ensembl
Innerchr19:48066441..48337397hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38270957
hg19270957
hg18270957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6474n54
Supporting Variantsnssv1149924
SamplesHGDP01378
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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