A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459963



Internal ID237965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177850000..177881324hg38UCSC Ensembl
chr5:177277001..177308325hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3831325
hg1931325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977676
Samples
Known GenesLOC728554
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459963
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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