A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434415



Internal ID22492285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107389239..107389332hg38UCSC Ensembl
chr7:107029684..107029777hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922874
Supporting Variants
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434415
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer