A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531634



Internal ID21855990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214013453..214013594hg38UCSC Ensembl
chr1:214186796..214186937hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982554
Supporting Variants
Samples
Known GenesPROX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531634
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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