A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002111



Internal ID21911454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121753564..121766074hg38UCSC Ensembl
chr10:123513079..123525589hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812511
hg1912511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592571
Samples
Known GenesATE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002111
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