A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433834



Internal ID21091387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121654501..121660300hg38UCSC Ensembl
chr8:122666741..122672540hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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