A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717268



Internal ID140934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34645773..34645827hg38UCSC Ensembl
chr18:32225737..32225791hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529558
Supporting Variants
Samples
Known GenesDTNA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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