A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367255



Internal ID22592924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45388050..45388140hg38UCSC Ensembl
chr11:45409601..45409691hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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