A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552042



Internal ID21876397
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 StatusS
Merged Variantsnsv6010453
Supporting Variants
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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