A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051444



Internal ID19140663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20401433hg38UCSC Ensembl
Innerchr15:20446126..20606686hg19UCSC Ensembl
Innerchr15:18706140..18866700hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38160561
hg19160561
hg18160561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2220n100
Supporting Variantsnssv3713619
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)nsv1051444
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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