A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841242



Internal ID22616177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119079904..119088942hg38UCSC Ensembl
chr5:118415599..118424637hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg389039
hg199039
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499979
Samples
Known GenesDMXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841242
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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