A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530201



Internal ID20903562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50907116..50951670hg38UCSC Ensembl
chr17:48984477..49029031hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3844555
hg1944555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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