A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018835



Internal ID19108052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:236075..526981hg38UCSC Ensembl
Innerchr9:236075..526981hg19UCSC Ensembl
Innerchr9:226075..516981hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38290907
hg19290907
hg18290907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7351n100
Supporting Variantsnssv3758070
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)nsv1018835
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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