A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841779



Internal ID22616714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139629739..139630738hg38UCSC Ensembl
chr5:139009324..139010323hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495580, nssv17495581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841779
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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