A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613081



Internal ID16400490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2024639..2044721hg38UCSC Ensembl
Innerchr9:2024639..2044721hg19UCSC Ensembl
Innerchr9:2014639..2034721hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3820083
hg1920083
hg1820083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156428
Samples1780862101_A
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613081
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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