A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855283



Internal ID22630218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134281488..134310339hg38UCSC Ensembl
chr11:134151382..134180233hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3828852
hg1928852
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454677, nssv17456445
Samples
Known GenesGLB1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855283
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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