A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743737



Internal ID20519726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143700689..143700891hg38UCSC Ensembl
chr5:143080254..143080456hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743737
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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