A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841075



Internal ID22616010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126777302..126778376hg38UCSC Ensembl
chr5:126112994..126114068hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494203, nssv17494204
Samples
Known GenesLMNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841075
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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