A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987894



Internal ID20554934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131316418..131338153hg38UCSC Ensembl
chr11:131186313..131208048hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3821736
hg1921736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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