A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606934



Internal ID21555239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152160908..152160908hg38UCSC Ensembl
chr2:153017422..153017422hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110325
SamplesHG01114
Known GenesSTAM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606934
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