A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291160



Internal ID20500378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174382770..174382770hg38UCSC Ensembl
chr4:175303921..175303921hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291160
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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