A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495349



Internal ID272467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35692768..35696761hg38UCSC Ensembl
chr13:36266905..36270898hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383994
hg193994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686856
Samples
Known GenesMIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495349
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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