A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073227



Internal ID21450247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:152420..152562hg38UCSC Ensembl
chr11:152420..152562hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600448
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073227
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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