A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988244



Internal ID20555284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134244801..134246700hg38UCSC Ensembl
chr11:134114695..134116594hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459187
Supporting Variants
Samples
Known GenesVPS26B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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