A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702566



Internal ID126232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83119383..83119536hg38UCSC Ensembl
chr15:83788135..83788288hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522247
Supporting Variants
Samples
Known GenesTM6SF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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