A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018439



Internal ID19107656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..518103hg38UCSC Ensembl
Innerchr9:46587..518103hg19UCSC Ensembl
Innerchr9:36587..508103hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38471517
hg19471517
hg18471517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7346n100
Supporting Variantsnssv3690958
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018439
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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