A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989432



Internal ID20556472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16039201..16042200hg38UCSC Ensembl
chr11:16060747..16063746hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450464
Supporting Variants
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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