A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026550



Internal ID19115768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..396380hg38UCSC Ensembl
Innerchr9:162695..396380hg19UCSC Ensembl
Innerchr9:152695..386380hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38233686
hg19233686
hg18233686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7350n100
Supporting Variantsnssv3690978
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026550
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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