A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643875



Internal ID21592180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117126450..117126450hg38UCSC Ensembl
chr10:118885961..118885961hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067564, nssv17067563
SamplesHG03009, HG00731
Known GenesKIAA1598
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643875
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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