A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442273



Internal ID21099826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110328204..110341325hg38UCSC Ensembl
chr10:112087962..112101083hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3813122
hg1913122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442273
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