A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765292



Internal ID20541152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31203675..31203675hg38UCSC Ensembl
chr4:31205297..31205297hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765292
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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