A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701292



Internal ID124958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54446874..54476874hg38UCSC Ensembl
chr15:54739072..54769072hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830001
hg1930001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519937
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701292
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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