A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841352



Internal ID22616287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119601298..119603049hg38UCSC Ensembl
chr5:118936993..118938744hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381752
hg191752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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