A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747874



Internal ID20523896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42158171..42158224hg38UCSC Ensembl
chr5:42158273..42158326hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273363
Samples
Known GenesLOC101926960
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747874
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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