A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408096



Internal ID21065649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63823459..63834063hg38UCSC Ensembl
chr5:63119286..63129890hg19UCSC Ensembl
Cytoband5q12.2
Allele length
AssemblyAllele length
hg3810605
hg1910605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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