A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436460



Internal ID21094013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51283607..51294055hg38UCSC Ensembl
chr10:53043367..53053815hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3810449
hg1910449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184233
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436460
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