A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410193



Internal ID21067746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152717583..152721311hg38UCSC Ensembl
chr5:152097143..152100871hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383729
hg193729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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