A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145426



Internal ID21510332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117121887..117121887hg38UCSC Ensembl
chr7:116761941..116761941hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639527
Supporting Variants
SamplesNA24385
Known GenesST7, ST7-AS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145426
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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