A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568380



Internal ID21516727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122705450..122705525hg38UCSC Ensembl
chr7:122345504..122345579hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141405
SamplesHG02587
Known GenesCADPS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568380
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer