A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423059



Internal ID21080612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112443335..112447421hg38UCSC Ensembl
chr8:113455564..113459650hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384087
hg194087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163560
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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