A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987135



Internal ID20554177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117105458..117106633hg38UCSC Ensembl
chr11:116976174..116977349hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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