A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071514



Internal ID21980747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103251070..103251070hg38UCSC Ensembl
chr8:104263298..104263298hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071514
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