A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046661



Internal ID19135880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20638246hg38UCSC Ensembl
Innerchr15:20216943..20843550hg19UCSC Ensembl
Innerchr15:18476957..19103564hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38626557
hg19626608
hg18626608
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2186n100
Supporting Variantsnssv3536960, nssv3715757, nssv3536959
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)nsv1046661
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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