A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076144



Internal ID21985377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193995718..193995718hg38UCSC Ensembl
chr3:193713507..193713507hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538745
Samples
Known GenesLOC647323
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076144
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer