A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843237



Internal ID22618172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87038725..87057662hg38UCSC Ensembl
chr5:86334542..86353479hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3818938
hg1918938
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843237
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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