A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148322



Internal ID15654822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136340055..136366634hg38UCSC Ensembl
Innerchr9:139234512..139261086hg19UCSC Ensembl
Innerchr9:138354333..138380907hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3826580
hg1926575
hg1826575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615962
Supporting Variants
Samples
Known GenesCARD9, DNLZ, GPSM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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