A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568178



Internal ID21760221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32965803..32965854hg38UCSC Ensembl
chr7:33005415..33005466hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012860
Supporting Variants
Samples
Known GenesFKBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568178
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