A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509019



Internal ID20882324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29199140..29208246hg38UCSC Ensembl
chr17:27526158..27535264hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389107
hg199107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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