A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465390



Internal ID243253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88547727..88547792hg38UCSC Ensembl
chr5:87843545..87843610hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968848
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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