A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530811



Internal ID21855167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204552364..204552454hg38UCSC Ensembl
chr1:204521492..204521582hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982419
Supporting Variants
Samples
Known GenesMDM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530811
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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