A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431286



Internal ID21088839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69862701..69865600hg38UCSC Ensembl
chr8:70774936..70777835hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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