A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052662



Internal ID19141881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20060713..20351177hg38UCSC Ensembl
Innerchr15:20265966..20556430hg19UCSC Ensembl
Innerchr15:18525980..18816444hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38290465
hg19290465
hg18290465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3538587
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)nsv1052662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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