A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530884



Internal ID21855240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11936772..11937100hg38UCSC Ensembl
chr1:11996829..11997157hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980790
Supporting Variants
Samples
Known GenesPLOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530884
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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