A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703351



Internal ID15093317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128569041..128609393hg38UCSC Ensembl
Innerchr9:131331320..131371672hg19UCSC Ensembl
Innerchr9:130371141..130411493hg18UCSC Ensembl
Innerchr9:128410874..128451226hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3840353
hg1940353
hg1840353
hg1740353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526979
Supporting Variants
Samples
Known GenesSPTAN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703351
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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