A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995769



Internal ID20562809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97259509..97366495hg38UCSC Ensembl
chr11:97130509..97237495hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38106987
hg19106987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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