A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690994



Internal ID114660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87295374..87444401hg38UCSC Ensembl
chr13:87947629..88096656hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38149028
hg19149028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501468
Supporting Variants
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690994
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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