A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585543



Internal ID21534091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78459168..78459522hg38UCSC Ensembl
chr11:78170214..78170568hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076782
SamplesHG02011
Known GenesNARS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585543
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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