A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000126



Internal ID21909469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43087503..43087953hg38UCSC Ensembl
chr5:43087605..43088055hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550060
Samples
Known GenesLOC100506639
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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