A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053556



Internal ID19142775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20384895hg38UCSC Ensembl
Innerchr15:20203949..20590148hg19UCSC Ensembl
Innerchr15:18463963..18850162hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38386200
hg19386200
hg18386200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n100
Supporting Variantsnssv3534496
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)nsv1053556
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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