A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981494



Internal ID21890837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162693432..162694570hg38UCSC Ensembl
chr1:162663222..162664360hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533319
Samples
Known GenesDDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981494
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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