A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513172



Internal ID289704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96945723..96946036hg38UCSC Ensembl
chr13:97597977..97598290hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694045
Samples
Known GenesLINC00359
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513172
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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