A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037941



Internal ID18780472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44860173..45003903hg38UCSC Ensembl
Innerchr15:45152371..45296101hg19UCSC Ensembl
Innerchr15:42939663..43083393hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38143731
hg19143731
hg18143731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2590n100
Supporting Variantsnssv3552360
Samples
Known GenesC15orf43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037941
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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