A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449534



Internal ID21107087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4840623..4846252hg38UCSC Ensembl
chr10:4882815..4888444hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385630
hg195630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181832
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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