A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405013



Internal ID21062566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114780529..114807831hg38UCSC Ensembl
chr5:114116226..114143528hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3827303
hg1927303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405013
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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