A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123607



Internal ID21475444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25596671..25596807hg38UCSC Ensembl
chr4:25598293..25598429hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582491
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123607
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