A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423886



Internal ID21081439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31020575..31021188hg38UCSC Ensembl
chr8:30878091..30878704hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165891
Samples
Known GenesPURG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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