A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036351



Internal ID19125570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129850799..129866907hg38UCSC Ensembl
Innerchr9:132613078..132629186hg19UCSC Ensembl
Innerchr9:131652899..131669007hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3816109
hg1916109
hg1816109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759827
Samples
Known GenesUSP20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036351
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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