A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429223



Internal ID21086776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96310004..96310505hg38UCSC Ensembl
chr8:97322232..97322733hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173778
Samples
Known GenesPTDSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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