A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999014



Internal ID21908357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16535659..16535735hg38UCSC Ensembl
chr5:16535768..16535844hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548547
Samples
Known GenesFAM134B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999014
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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