A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121267



Internal ID21477551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41061933..41062122hg38UCSC Ensembl
chr5:41062035..41062224hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571818
Supporting Variants
SamplesHG03486
Known GenesMROH2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121267
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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