A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013262



Internal ID21922605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28103101..28103155hg38UCSC Ensembl
chr10:28392030..28392084hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585401
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013262
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