A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738796



Internal ID20514767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181253132..181254470hg38UCSC Ensembl
chr5:180680132..180681470hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381339
hg191339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738796
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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