A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610960



Internal ID21559265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26652243..26652243hg38UCSC Ensembl
chr4:26653865..26653865hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138369
SamplesNA20847
Known GenesTBC1D19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610960
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