A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613080



Internal ID16400489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2018825..2066493hg38UCSC Ensembl
Innerchr9:2018825..2066493hg19UCSC Ensembl
Innerchr9:2008825..2056493hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3847669
hg1947669
hg1847669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12467n54
Supporting Variantsnssv1156427
Samples1780862414_A
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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