A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365081



Internal ID22590750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5476751..5477270hg38UCSC Ensembl
chr11:5497981..5498500hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908296
Supporting Variants
Samples
Known GenesOR51B5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365081
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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