A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843193



Internal ID22618128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83126021..83133212hg38UCSC Ensembl
chr5:82421840..82429031hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg387192
hg197192
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500356
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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