A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523894



Internal ID21848253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27160908..27160991hg38UCSC Ensembl
chr1:27487399..27487482hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983507
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523894
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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