A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983601



Internal ID56445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35501538..35501624hg38UCSC Ensembl
chr6:35469315..35469401hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471897
Supporting Variants
Samples
Known GenesTULP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983601
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.035178


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