A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905451



Internal ID22680638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176371498..176371573hg38UCSC Ensembl
chr5:175798501..175798576hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422016
Samples
Known GenesARL10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905451
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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