A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495501



Internal ID272611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25034078..25035210hg38UCSC Ensembl
chr13:25608216..25609348hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381133
hg191133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495501
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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