A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508974



Internal ID285647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53370215..53384120hg38UCSC Ensembl
chr13:53944350..53958255hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3813906
hg1913906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508974
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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