A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569643



Internal ID21518004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41531538..41531631hg38UCSC Ensembl
chr1:41997209..41997302hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065758
SamplesHG00731
Known GenesHIVEP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569643
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