A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620711



Internal ID21569016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14152137..14152137hg38UCSC Ensembl
chr3:14193637..14193637hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133082
SamplesHG00171
Known GenesXPC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620711
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