A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511687



Internal ID20885017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42852909..42868831hg38UCSC Ensembl
chr17:41004926..41020848hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3815923
hg1915923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035658
Samples
Known GenesAOC3, AOC4P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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