A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495960



Internal ID273053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25979003..25979105hg38UCSC Ensembl
chr13:26553141..26553243hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686360
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495960
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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