A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421691



Internal ID21079244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69948151..69958341hg38UCSC Ensembl
chr8:70860386..70870576hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3810191
hg1910191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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