A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433237



Internal ID21090790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96310254..96310927hg38UCSC Ensembl
chr8:97322482..97323155hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226843
Samples
Known GenesPTDSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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