A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051781



Internal ID19141000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20381394hg38UCSC Ensembl
Innerchr15:20284054..20586647hg19UCSC Ensembl
Innerchr15:18544068..18846661hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38302594
hg19302594
hg18302594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3540026, nssv3540027
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)nsv1051781
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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