A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529311



Internal ID21853668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74176298..74176470hg38UCSC Ensembl
chr2:74403425..74403597hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989898
Supporting Variants
Samples
Known GenesMOB1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529311
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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