A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528841



Internal ID21853198
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 StatusS
Merged Variantsnsv5981344
Supporting Variants
Samples
Known GenesDDAH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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