A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456021



Internal ID234090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117465496..117466157hg38UCSC Ensembl
chr5:116801192..116801853hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972765
Samples
Known GenesLINC00992
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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