A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036559



Internal ID19125778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20773569hg38UCSC Ensembl
Innerchr15:20446126..20978898hg19UCSC Ensembl
Innerchr15:18706140..19238943hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38532697
hg19532773
hg18532804
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2209n100
Supporting Variantsnssv3713630, nssv3534729
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)nsv1036559
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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