A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574674



Internal ID21766717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117619858..117620191hg38UCSC Ensembl
chr7:117259912..117260245hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000672
Supporting Variants
Samples
Known GenesCFTR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574674
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