A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014829



Internal ID21924172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28771966..28772130hg38UCSC Ensembl
chr10:29060895..29061059hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014829
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