A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536208



Internal ID21860563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36139201..36139281hg38UCSC Ensembl
chr1:36604802..36604882hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984194
Supporting Variants
Samples
Known GenesTRAPPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536208
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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