A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675617



Internal ID15412269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130144207..130216809hg38UCSC Ensembl
Innerchr9:132906486..132979088hg19UCSC Ensembl
Innerchr9:131946307..132018909hg18UCSC Ensembl
Innerchr9:129986040..130058642hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3872603
hg1972603
hg1872603
hg1772603
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)nssv675617
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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