A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999466



Internal ID21908809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:357691..358106hg38UCSC Ensembl
chr5:357806..358221hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551028
Samples
Known GenesAHRR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999466
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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