A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051798



Internal ID18794329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68896889..69177116hg38UCSC Ensembl
Innerchr9:71511805..71792032hg19UCSC Ensembl
Innerchr9:70701625..70981852hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38280228
hg19280228
hg18280228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7666n100
Supporting Variantsnssv3696220
Samples
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051798
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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