A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419252



Internal ID21076805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66113364..66113985hg38UCSC Ensembl
chr8:67025599..67026220hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419252
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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