A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701406



Internal ID125072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34296321..34300665hg38UCSC Ensembl
chr15:34588522..34592866hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384345
hg194345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499269
Supporting Variants
Samples
Known GenesSLC12A6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701406
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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