A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1144791



Internal ID15997977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129435856..129454751hg38UCSC Ensembl
Innerchr9:132198135..132217030hg19UCSC Ensembl
Innerchr9:131237956..131256851hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3818896
hg1918896
hg1818896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615441
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)nssv1144791
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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