A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988002



Internal ID20555042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128039949..128040765hg38UCSC Ensembl
chr11:127909844..127910660hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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