A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539747



Internal ID21864102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55247167..55249183hg38UCSC Ensembl
chr5:54542995..54545011hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539747
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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