A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453633



Internal ID21111186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122478215..122566019hg38UCSC Ensembl
chr10:124237731..124325535hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3887805
hg1987805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177204
Samples
Known GenesDMBT1, HTRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453633
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