A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405768



Internal ID21063321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87573135..87769194hg38UCSC Ensembl
chr5:86868952..87065011hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38196060
hg19196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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