A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034067



Internal ID21943410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89935592..90135843hg38UCSC Ensembl
chr11:89668760..89869011hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38200252
hg19200252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585735
Samples
Known GenesMIR5692A1, NAALAD2, TRIM49C, TRIM53AP, TRIM64, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034067
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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