A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456599



Internal ID234661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170262220..170262271hg38UCSC Ensembl
chr5:169689224..169689275hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976658
Samples
Known GenesLCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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