A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980519



Internal ID21889862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11033593..11033875hg38UCSC Ensembl
chr1:11093650..11093932hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535832
Samples
Known GenesMASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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