A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040900



Internal ID18783431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34376855..34740872hg38UCSC Ensembl
Innerchr15:34669056..35033073hg19UCSC Ensembl
Innerchr15:32456348..32820365hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38364018
hg19364018
hg18364018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2552n100
Supporting Variantsnssv3547877
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040900
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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