A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740256



Internal ID20516231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39053735..39053925hg38UCSC Ensembl
chr5:39053837..39054027hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278596
Samples
Known GenesRICTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740256
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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