A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496386



Internal ID20869588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:831801..895100hg38UCSC Ensembl
chr17:735041..798340hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3863300
hg1963300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195701
Samples
Known GenesNXN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496386
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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