A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429320



Internal ID21086873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25712701..25735600hg38UCSC Ensembl
chr8:25570217..25593116hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3822900
hg1922900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429320
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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