A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420740



Internal ID21078293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22596376..22598801hg38UCSC Ensembl
chr8:22453889..22456314hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167103
Samples
Known GenesPDLIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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