A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467918



Internal ID22525807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131161981..131163555hg38UCSC Ensembl
chr11:131031876..131033450hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467918
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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