A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694491



Internal ID118157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95252626..95252724hg38UCSC Ensembl
chr13:95904880..95904978hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510612
Supporting Variants
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694491
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001717


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