A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758056



Internal ID19056337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..289419hg38UCSC Ensembl
Innerchr9:46587..289419hg19UCSC Ensembl
Innerchr9:36587..279419hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38242833
hg19242833
hg18242833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015933
Supporting Variants
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)nssv3758056
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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