A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033923



Internal ID19123145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..322795hg38UCSC Ensembl
Innerchr9:46587..322795hg19UCSC Ensembl
Innerchr9:36587..312795hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38276209
hg19276209
hg18276209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7344n100
Supporting Variantsnssv3690949, nssv3690950
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)nsv1033923
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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