A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535294



Internal ID310949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27987977..27988027hg38UCSC Ensembl
chr13:28562114..28562164hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686450
Samples
Known GenesURAD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535294
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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