A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124691



Internal ID21497168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194311184..194311184hg38UCSC Ensembl
chr3:194028973..194028973hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605396
Supporting Variants
SamplesNA19238
Known GenesLINC00887
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124691
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