A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853701



Internal ID22628636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1247706..1250018hg38UCSC Ensembl
chr11:1268936..1271248hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459690, nssv17458386
Samples
Known GenesMUC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853701
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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