A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852543



Internal ID22627478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102868435..102870302hg38UCSC Ensembl
chr11:102739165..102741032hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381868
hg191868
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450503
Samples
Known GenesMMP12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852543
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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