A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426687



Internal ID21084240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49771067..49771744hg38UCSC Ensembl
chr8:50683627..50684304hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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