A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054418



Internal ID18796949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44860173..44997558hg38UCSC Ensembl
Innerchr15:45152371..45289756hg19UCSC Ensembl
Innerchr15:42939663..43077048hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38137386
hg19137386
hg18137386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2590n100
Supporting Variantsnssv3552358, nssv3552357, nssv3552356, nssv3552359
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)nsv1054418
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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