A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143739



Internal ID21453572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107532997..107535572hg38UCSC Ensembl
chr7:107173442..107176017hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382576
hg192576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578284
Supporting Variants
SamplesHG02011
Known GenesCOG5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143739
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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