A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401827



Internal ID21059380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117277427..117277930hg38UCSC Ensembl
chr5:116613123..116613626hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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