A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530771



Internal ID21855127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219358143..219358348hg38UCSC Ensembl
chr1:219531485..219531690hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530771
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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