A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702009



Internal ID125675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43364405..43364505hg38UCSC Ensembl
chr15:43656603..43656703hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498962
Supporting Variants
Samples
Known GenesZSCAN29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702009
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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