A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139082



Internal ID15992268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86945922..86946639hg38UCSC Ensembl
Innerchr9:89560837..89561554hg19UCSC Ensembl
Innerchr9:88750657..88751374hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38718
hg19718
hg18718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614783
Supporting Variants
Samples
Known GenesGAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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