A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925782



Internal ID22701009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1251987..1252086hg38UCSC Ensembl
chr11:1273217..1273316hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366430
Samples
Known GenesMUC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925782
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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