A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686189



Internal ID109855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23874301..23874441hg38UCSC Ensembl
chr13:24448440..24448580hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494085
Supporting Variants
Samples
Known GenesMIPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686189
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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