A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426665



Internal ID21084218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111584209..112563698hg38UCSC Ensembl
chr8:112596438..113575927hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38979490
hg19979490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163061
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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