A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130503



Internal ID21489833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14116109..14116109hg38UCSC Ensembl
chr4:14117733..14117733hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621473
Supporting Variants
SamplesNA19238
Known GenesLINC01085
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130503
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