A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037818



Internal ID21947161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67262430..67262657hg38UCSC Ensembl
chr17:65258546..65258773hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037818
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