A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544062



Internal ID21868417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83126067..83126067hg38UCSC Ensembl
chr5:82421886..82421886hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063271
Supporting Variants
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544062
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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