A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410898



Internal ID21068451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110414207..110515784hg38UCSC Ensembl
chr5:109749908..109851485hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38101578
hg19101578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124867
Samples
Known GenesTMEM232
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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