A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134121



Internal ID15987307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67330186..67423306hg38UCSC Ensembl
Innerchr9:40064995..40162120hg19UCSC Ensembl
Innerchr9:40054995..40152120hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3893121
hg1997126
hg1897126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614304
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)nssv1134121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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