A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010453



Internal ID21919796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83126067..83128862hg38UCSC Ensembl
chr5:82421886..82424681hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg382796
hg192796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552042
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010453
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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