A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502157



Internal ID20875399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54597374..55150720hg38UCSC Ensembl
chr15:54889572..55442918hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38553347
hg19553347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187758
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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