A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015376



Internal ID18757910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4686223..4737890hg38UCSC Ensembl
Innerchr9:4686223..4737890hg19UCSC Ensembl
Innerchr9:4676223..4727890hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3851668
hg1951668
hg1851668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692395
Samples
Known GenesAK3, CDC37L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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