A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042655



Internal ID19131874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20368091hg38UCSC Ensembl
Innerchr15:20203949..20573344hg19UCSC Ensembl
Innerchr15:18463963..18833358hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38369396
hg19369396
hg18369396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n100
Supporting Variantsnssv3534472
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)nsv1042655
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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