A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408152



Internal ID21065705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15073080..15100878hg38UCSC Ensembl
chr6:15073311..15101109hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3827799
hg1927799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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