A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686545



Internal ID110211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29641700..29647707hg38UCSC Ensembl
chr13:30215837..30221844hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686545
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.540287


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