A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039761



Internal ID18782292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90836574..90915549hg38UCSC Ensembl
Innerchr9:93598856..93677831hg19UCSC Ensembl
Innerchr9:92638677..92717652hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3878976
hg1978976
hg1878976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7687n100
Supporting Variantsnssv3697545
Samples
Known GenesSYK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039761
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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