A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400589



Internal ID21058142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87458214..87506634hg38UCSC Ensembl
chr5:86754031..86802451hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3848421
hg1948421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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