A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141630



Internal ID15648130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127741791..127824409hg38UCSC Ensembl
Innerchr9:130504070..130586688hg19UCSC Ensembl
Innerchr9:129543891..129626509hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3882619
hg1982619
hg1882619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615372
Supporting Variants
Samples
Known GenesCDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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