A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451590



Internal ID21109143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112796289..112807736hg38UCSC Ensembl
chr10:114556048..114567495hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3811448
hg1911448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179865
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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