A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543411



Internal ID21867766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53102580..53102634hg38UCSC Ensembl
chr5:52398410..52398464hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999968
Supporting Variants
Samples
Known GenesMOCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543411
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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