A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039345



Internal ID19128564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20738717hg38UCSC Ensembl
Innerchr15:20284054..20944046hg19UCSC Ensembl
Innerchr15:18544068..19204074hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38659917
hg19659993
hg18660007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2201n100
Supporting Variantsnssv3715981
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039345
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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