A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841655



Internal ID22616590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130960991..131025851hg38UCSC Ensembl
chr5:130296684..130361544hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3864861
hg1964861
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841655
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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