A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035498



Internal ID19124717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20657723hg38UCSC Ensembl
Innerchr15:20216943..20863052hg19UCSC Ensembl
Innerchr15:18476957..19123066hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38646034
hg19646110
hg18646110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2187n100
Supporting Variantsnssv3715758
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035498
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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