A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149220



Internal ID21508793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:410974..411044hg38UCSC Ensembl
chr7:450940..451010hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568255
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149220
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