A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1144778



Internal ID15997964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129377690..129417950hg38UCSC Ensembl
Innerchr9:132139969..132180229hg19UCSC Ensembl
Innerchr9:131179790..131220050hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3840261
hg1940261
hg1840261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615424
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)nssv1144778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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