A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456377



Internal ID234447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160558872..160608084hg38UCSC Ensembl
chr5:159985879..160035091hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3849213
hg1949213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976948
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456377
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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