A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417086



Internal ID21074639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112062470..112173299hg38UCSC Ensembl
chr8:113074699..113185528hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38110830
hg19110830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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