A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520969



Internal ID21845328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153822030..153824465hg38UCSC Ensembl
chr1:153794506..153796941hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382436
hg192436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981633
Supporting Variants
Samples
Known GenesGATAD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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