A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520511



Internal ID20893872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50399585..50405604hg38UCSC Ensembl
chr17:48476946..48482965hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg386020
hg196020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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