A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994120



Internal ID20561160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65461493..65467184hg38UCSC Ensembl
chr11:65228964..65234655hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385692
hg195692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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