A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016104



Internal ID21925447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14872087..14872228hg38UCSC Ensembl
chr10:14914086..14914227hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016104
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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