A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154876



Internal ID22085381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19502948..20032175hg38UCSC Ensembl
Outerchr13:19495623..20034420hg38UCSC Ensembl
Innerchr13:20077088..20606315hg19UCSC Ensembl
Outerchr13:20069763..20608560hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38538798
hg19538798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010398
Samples
Known GenesMPHOSPH8, PSPC1, TPTE2, ZMYM2, ZMYM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154876
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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