A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063023



Internal ID21972256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70029291..70029291hg38UCSC Ensembl
chr4:70895008..70895008hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555641
Samples
Known GenesHTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063023
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