A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456086



Internal ID234157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2411305..2411398hg38UCSC Ensembl
chr5:2411419..2411512hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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