A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426953



Internal ID21084506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111343270..111443665hg38UCSC Ensembl
chr8:112355499..112455894hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38100396
hg19100396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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