A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986402



Internal ID20553442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109008438..109012174hg38UCSC Ensembl
chr11:108879165..108882901hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383737
hg193737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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