A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410253



Internal ID21067806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80763047..80766483hg38UCSC Ensembl
chr5:80058866..80062302hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134121
Samples
Known GenesMSH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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