A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840663



Internal ID22615598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111537152..111538351hg38UCSC Ensembl
chr5:110872850..110874049hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493069
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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