A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126532



Internal ID15633032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5841438..5877948hg38UCSC Ensembl
Innerchr9:5841438..5877948hg19UCSC Ensembl
Innerchr9:5831438..5867948hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3836511
hg1936511
hg1836511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613203
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126532
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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