A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518446



Internal ID20891807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67989396..68001680hg38UCSC Ensembl
chr17:65985512..65997796hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3812285
hg1912285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037447
Samples
Known GenesC17orf58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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