A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145397



Internal ID15651897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133090975..133147666hg38UCSC Ensembl
Innerchr9:135966362..136023053hg19UCSC Ensembl
Innerchr9:134956183..135012874hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3856692
hg1956692
hg1856692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615607
Supporting Variants
Samples
Known GenesRALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145397
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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