A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842852



Internal ID22617787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67763553..67765552hg38UCSC Ensembl
chr5:67059381..67061380hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498082, nssv17498083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842852
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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