A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155381



Internal ID21488551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53932768..53932768hg38UCSC Ensembl
chr7:54000461..54000461hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635849
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155381
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