A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535117



Internal ID20908478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65421628..65425751hg38UCSC Ensembl
chr17:63417746..63421869hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg384124
hg194124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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