A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993674



Internal ID20560714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58021041..58025005hg38UCSC Ensembl
chr11:57788513..57792477hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg383965
hg193965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461436
Supporting Variants
Samples
Known GenesOR9Q1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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