A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981344



Internal ID21890687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145522721..145549431hg38UCSC Ensembl
chr1:85980531..86005692hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3826711
hg1925162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528841
Samples
Known GenesDDAH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981344
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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