A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553579



Internal ID326812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142537962..142537962hg38UCSC Ensembl
chr5:141917527..141917527hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553579
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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