A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421874



Internal ID21079427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9740241..9742803hg38UCSC Ensembl
chr8:9597751..9600313hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382563
hg192563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173535
Samples
Known GenesMIR597, TNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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