A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453512



Internal ID21111065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102451952..102452409hg38UCSC Ensembl
chr10:104211709..104212166hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977264
Samples
Known GenesLOC100505761
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453512
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