A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408301



Internal ID21065854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132406251..132410623hg38UCSC Ensembl
chr5:131741943..131746315hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384373
hg194373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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