A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013824



Internal ID21923167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10292263..10294427hg38UCSC Ensembl
chr10:10334226..10336390hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013824
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