A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1144781



Internal ID15997967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129385533..129408394hg38UCSC Ensembl
Innerchr9:132147812..132170673hg19UCSC Ensembl
Innerchr9:131187633..131210494hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3822862
hg1922862
hg1822862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615429
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)nssv1144781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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