A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076815



Internal ID21986048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121182517..121182517hg38UCSC Ensembl
chr4:122103672..122103672hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554210
Samples
Known GenesTNIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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