A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461716



Internal ID239662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127373884..127378660hg38UCSC Ensembl
chr6:127695029..127699805hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg384777
hg194777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461716
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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