A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912882



Internal ID22688098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72099255..72103180hg38UCSC Ensembl
chr11:71810301..71814226hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383926
hg193926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349984
Samples
Known GenesLAMTOR1, LRTOMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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