A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701729



Internal ID15438381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130187585..130200850hg38UCSC Ensembl
Innerchr9:132949864..132963129hg19UCSC Ensembl
Innerchr9:131989685..132002950hg18UCSC Ensembl
Innerchr9:130029418..130042683hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813266
hg1913266
hg1813266
hg1713266
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520802
Supporting Variants
Samples
Known GenesNCS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701729
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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