A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287644



Internal ID20496862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117926127..117926243hg38UCSC Ensembl
chr11:117796842..117796958hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741952
Supporting Variants
Samples
Known GenesTMPRSS13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287644
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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