A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036217



Internal ID19125436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..20381394hg38UCSC Ensembl
Innerchr15:20291301..20586647hg19UCSC Ensembl
Innerchr15:18551315..18846661hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38295347
hg19295347
hg18295347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3537914
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)nsv1036217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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