A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419311



Internal ID21076864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82328618..82403025hg38UCSC Ensembl
chr8:83240853..83315260hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3874408
hg1974408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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