A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525499



Internal ID20898860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79696267..79697925hg38UCSC Ensembl
chr17:77670191..77671839hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381659
hg191649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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