A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989903



Internal ID20556943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36101936..36103251hg38UCSC Ensembl
chr11:36123486..36124801hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463093
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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