A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994657



Internal ID20561697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87002343..87004612hg38UCSC Ensembl
chr11:86713385..86715654hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382270
hg192270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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