A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015879



Internal ID19105097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..360382hg38UCSC Ensembl
Innerchr9:46587..360382hg19UCSC Ensembl
Innerchr9:36587..350382hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38313796
hg19313796
hg18313796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7345n100
Supporting Variantsnssv3690951
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)nsv1015879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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