A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989782



Internal ID20556822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26921090..26921407hg38UCSC Ensembl
chr11:26942637..26942954hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00197


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