A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141292



Internal ID15994478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118033712..118127688hg38UCSC Ensembl
Innerchr9:120795990..120889966hg19UCSC Ensembl
Innerchr9:119835811..119929787hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3893977
hg1993977
hg1893977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615265
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)nssv1141292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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