A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686699



Internal ID110365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32042487..32042552hg38UCSC Ensembl
chr13:32616624..32616689hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498344
Supporting Variants
Samples
Known GenesFRY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.047954


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