A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737887



Internal ID20513852
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 StatusM
Merged Variants
Supporting Variantsnssv16272551
Samples
Known GenesARHGEF28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737887
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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