A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272551



Internal ID20481769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73775878..73775930hg38UCSC Ensembl
chr5:73071703..73071755hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737887
Supporting Variants
Samples
Known GenesARHGEF28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272551
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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