A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027206



Internal ID19116425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:236075..499586hg38UCSC Ensembl
Innerchr9:236075..499586hg19UCSC Ensembl
Innerchr9:226075..489586hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38263512
hg19263512
hg18263512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7351n100
Supporting Variantsnssv3691003
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)nsv1027206
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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