A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980938



Internal ID21890281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118877954..118881658hg38UCSC Ensembl
chr1:119420577..119424281hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg383705
hg193705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980938
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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