A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156848



Internal ID21482759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98452188..98452188hg38UCSC Ensembl
chr7:98081500..98081500hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641981
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156848
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