A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406638



Internal ID21064191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155832686..155835323hg38UCSC Ensembl
chr5:155259696..155262333hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382638
hg192638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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