A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501694



Internal ID20874931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11831584..11832165hg38UCSC Ensembl
chr17:11734901..11735482hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033718
Samples
Known GenesDNAH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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