A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145116



Internal ID15651616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129654635..129711337hg38UCSC Ensembl
Innerchr9:132416914..132473616hg19UCSC Ensembl
Innerchr9:131456735..131513437hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3856703
hg1956703
hg1856703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615496
Supporting Variants
Samples
Known GenesPRRX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145116
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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