A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536397



Internal ID21860752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168207931..168208012hg38UCSC Ensembl
chr1:168177169..168177250hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536397
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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