A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508536



Internal ID20881838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14544564..14553205hg38UCSC Ensembl
chr17:14447881..14456522hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg388642
hg198642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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