A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573680



Internal ID21765723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17338153..17338211hg38UCSC Ensembl
chr7:17377777..17377835hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001275
Supporting Variants
Samples
Known GenesAHR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573680
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