A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368784



Internal ID22594453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59798463..59798781hg38UCSC Ensembl
chr11:59565936..59566254hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910908
Supporting Variants
Samples
Known GenesSTX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368784
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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