A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988238



Internal ID20555278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134164592..134165904hg38UCSC Ensembl
chr11:134034487..134035799hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461105
Supporting Variants
Samples
Known GenesNCAPD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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