A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014231



Internal ID21923574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80788523..80834194hg38UCSC Ensembl
chr5:80084342..80130013hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3845672
hg1945672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546382
Samples
Known GenesMSH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014231
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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