A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855608



Internal ID22630543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127767309..127774334hg38UCSC Ensembl
chr11:127637204..127644229hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387026
hg197026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv294n209
Supporting Variantsnssv17451355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855608
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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