A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047299



Internal ID19136518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20372432hg38UCSC Ensembl
Innerchr15:20216943..20577685hg19UCSC Ensembl
Innerchr15:18476957..18837699hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38360743
hg19360743
hg18360743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n100
Supporting Variantsnssv3535730
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047299
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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