A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043476



Internal ID21952780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27419550..27419550hg38UCSC Ensembl
chr3:27461041..27461041hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553067
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043476
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