A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741432



Internal ID20517409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8026905..8027212hg38UCSC Ensembl
chr5:8027018..8027325hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741432
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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