A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765938



Internal ID20541798
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 StatusM
Merged Variants
Supporting Variantsnssv16291160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765938
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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