A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540361



Internal ID315148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44936847..44936857hg38UCSC Ensembl
chr5:44936949..44936959hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540361
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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