A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076494



Internal ID21985727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119796374..119796374hg38UCSC Ensembl
chr4:120717529..120717529hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076494
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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