A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553663



Internal ID326891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52675987..52675987hg38UCSC Ensembl
chr10:54435747..54435747hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553663
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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