A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694090



Internal ID15430742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130156951..130157174hg38UCSC Ensembl
Innerchr9:132919230..132919453hg19UCSC Ensembl
Innerchr9:131959051..131959274hg18UCSC Ensembl
Innerchr9:129998784..129999007hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38224
hg19224
hg18224
hg17224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520802
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694090
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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