A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063271



Internal ID21972504
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 StatusM
Merged Variants
Supporting Variantsnssv17544062
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063271
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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