A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843434



Internal ID22618369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79221007..79222756hg38UCSC Ensembl
chr5:78516830..78518579hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843434
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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