A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017197



Internal ID19106414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:325877..519256hg38UCSC Ensembl
Innerchr9:325877..519256hg19UCSC Ensembl
Innerchr9:315877..509256hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38193380
hg19193380
hg18193380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7359n100
Supporting Variantsnssv3691016
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)nsv1017197
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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