A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986445



Internal ID20553485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109525201..109530200hg38UCSC Ensembl
chr11:109395927..109400926hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00423


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