A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843119



Internal ID22618054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63565201..63569250hg38UCSC Ensembl
chr5:62861028..62865077hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499894, nssv17498027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843119
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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