A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450055



Internal ID21107608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59331399..59332027hg38UCSC Ensembl
chr10:61091159..61091787hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983211
Samples
Known GenesFAM13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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