A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533143



Internal ID20906504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77788774..77819145hg38UCSC Ensembl
chr17:75784856..75815227hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3830372
hg1930372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533143
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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