A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016807



Internal ID19106024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:424875..480955hg38UCSC Ensembl
Innerchr9:424875..480955hg19UCSC Ensembl
Innerchr9:414875..470955hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3856081
hg1956081
hg1856081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691022
Samples
Known GenesDOCK8, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016807
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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