A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702396



Internal ID126062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71688336..71699292hg38UCSC Ensembl
chr15:71980675..71991631hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3810957
hg1910957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146143
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702396
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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