A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535491



Internal ID20908852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65142080..65146336hg38UCSC Ensembl
chr17:63138198..63142454hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg384257
hg194257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037824
Samples
Known GenesRGS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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