A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438622



Internal ID21096175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28425868..28429286hg38UCSC Ensembl
chr10:28714797..28718215hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383419
hg193419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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