A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019991



Internal ID19109210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:295237..533926hg38UCSC Ensembl
Innerchr9:295237..533926hg19UCSC Ensembl
Innerchr9:285237..523926hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38238690
hg19238690
hg18238690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7359n100
Supporting Variantsnssv3691012
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)nsv1019991
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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