A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911768



Internal ID22686983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62407876..62413715hg38UCSC Ensembl
chr10:64167635..64173474hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385840
hg195840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357033
Samples
Known GenesZNF365
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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