A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540967



Internal ID315646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161632444..161632444hg38UCSC Ensembl
chr5:161059450..161059450hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540967
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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