A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840722



Internal ID22615657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119153597..119155096hg38UCSC Ensembl
chr5:118489292..118490791hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493767
Samples
Known GenesDMXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840722
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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