A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136069



Internal ID21502603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151777918..151777918hg38UCSC Ensembl
chr5:151157479..151157479hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629690
Supporting Variants
SamplesNA19239
Known GenesG3BP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136069
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