A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432619



Internal ID21090172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114073935..114074628hg38UCSC Ensembl
chr8:115086164..115086857hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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