A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019576



Internal ID21928919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149327060..149327300hg38UCSC Ensembl
chr5:148706623..148706863hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565596
Samples
Known GenesAFAP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019576
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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