A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351932



Internal ID22577601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128450201..128452353hg38UCSC Ensembl
chr11:128320096..128322248hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382153
hg192153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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