A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054671



Internal ID19143890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41723899..41806698hg38UCSC Ensembl
Innerchr15:42016097..42098896hg19UCSC Ensembl
Innerchr15:39803389..39886188hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3882800
hg1982800
hg1882800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2581n100
Supporting Variantsnssv3552263
Samples
Known GenesMAPKBP1, MGA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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