A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432568



Internal ID21090121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100886840..100906347hg38UCSC Ensembl
chr8:101899068..101918575hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3819508
hg1919508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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