A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745730



Internal ID20521740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173445715..173445873hg38UCSC Ensembl
chr4:174366866..174367024hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745730
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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