A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988663



Internal ID20555703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18643315..18649083hg38UCSC Ensembl
chr11:18664862..18670630hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385769
hg195769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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