A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634074



Internal ID21582379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15694354..15694354hg38UCSC Ensembl
chr10:15736353..15736353hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069261
SamplesHG03732
Known GenesITGA8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634074
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