A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033678



Internal ID19122899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..319961hg38UCSC Ensembl
Innerchr9:46587..319961hg19UCSC Ensembl
Innerchr9:36587..309961hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38273375
hg19273375
hg18273375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7344n100
Supporting Variantsnssv3690948
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033678
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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