A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144318



Internal ID21475927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132151577..132151577hg38UCSC Ensembl
chr7:131836336..131836336hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636790
Supporting Variants
SamplesHG03486
Known GenesPLXNA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144318
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