A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154331



Internal ID21451831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55210476..55210476hg38UCSC Ensembl
chr7:55278169..55278169hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627678
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154331
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