A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843441



Internal ID22618376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82270254..82273679hg38UCSC Ensembl
chr5:81566073..81569498hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg383426
hg193426
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498794
Samples
Known GenesRPS23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843441
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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