A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545873



Internal ID21870228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51535796..51535868hg38UCSC Ensembl
chr5:50831630..50831702hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545873
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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