A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046483



Internal ID98794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72097917..72098286hg38UCSC Ensembl
chr11:71808963..71809332hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501878
Supporting Variants
Samples
Known GenesLAMTOR1, LRTOMT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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