A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501380



Internal ID20874613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17389478..17397765hg38UCSC Ensembl
chr17:17292792..17301079hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg388288
hg198288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501380
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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