A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430360



Internal ID21087913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50962417..51288744hg38UCSC Ensembl
chr8:51874977..52201304hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38326328
hg19326328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430360
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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