A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1144779



Internal ID15997965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129377690..129419493hg38UCSC Ensembl
Innerchr9:132139969..132181772hg19UCSC Ensembl
Innerchr9:131179790..131221593hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3841804
hg1941804
hg1841804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615425
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)nssv1144779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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