A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535506



Internal ID20908867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49272602..49275737hg38UCSC Ensembl
chr17:47349964..47353099hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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