A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990887



Internal ID20557927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35056827..35066810hg38UCSC Ensembl
chr11:35078374..35088357hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389984
hg199984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472797
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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