A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447375



Internal ID21104928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113602884..113688099hg38UCSC Ensembl
chr10:115362643..115447858hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3885216
hg1985216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192035
Samples
Known GenesCASP7, NRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447375
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