A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417731



Internal ID21075284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83736588..83742015hg38UCSC Ensembl
chr8:84648823..84654250hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg385428
hg195428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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