A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939599



Internal ID22714995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56780964..56943658hg38UCSC Ensembl
chr15:57073162..57235856hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38162695
hg19162695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386428
Samples
Known GenesLOC145783, TCF12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939599
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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