A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541677



Internal ID316252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38367469..38367513hg38UCSC Ensembl
chr20:36996113..36996157hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732306
Samples
Known GenesLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541677
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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