A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100072



Internal ID22009305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112056193..112056193hg38UCSC Ensembl
chr10:113815951..113815951hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100072
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