A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541620



Internal ID316199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52577090..52577141hg38UCSC Ensembl
chr6:52441888..52441939hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541620
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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