A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603497



Internal ID21552162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1250099..1250185hg38UCSC Ensembl
chr11:1271329..1271415hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073462
SamplesNA12878
Known GenesMUC5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603497
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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