A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425630



Internal ID21083183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9584149..9596075hg38UCSC Ensembl
chr8:9441659..9453585hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811927
hg1911927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173750
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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