A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026938



Internal ID21936281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74997021..75001288hg38UCSC Ensembl
chr17:72993116..72997383hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384268
hg194268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634327
Samples
Known GenesCDR2L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026938
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