A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434571



Internal ID21092124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8460175..8593160hg38UCSC Ensembl
chr8:8317685..8450670hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38132986
hg19132986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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