A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041613



Internal ID18784144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44819169..44992080hg38UCSC Ensembl
Innerchr15:45111367..45284278hg19UCSC Ensembl
Innerchr15:42898659..43071570hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38172912
hg19172912
hg18172912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2588n100
Supporting Variantsnssv3552349, nssv3552348
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)nsv1041613
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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