A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047353



Internal ID18789884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44813176..44997558hg38UCSC Ensembl
Innerchr15:45105374..45289756hg19UCSC Ensembl
Innerchr15:42892666..43077048hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38184383
hg19184383
hg18184383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2588n100
Supporting Variantsnssv3552344, nssv3552345, nssv3552346, nssv3552343
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)nsv1047353
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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