A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668871



Internal ID15058837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127260261..127273883hg38UCSC Ensembl
Innerchr9:130022540..130036162hg19UCSC Ensembl
Innerchr9:129062361..129075983hg18UCSC Ensembl
Innerchr9:127102094..127115716hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3813623
hg1913623
hg1813623
hg1713623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516966
Supporting Variants
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668871
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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