A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452538



Internal ID21110091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69630748..69653820hg38UCSC Ensembl
chr10:71390504..71413576hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3823073
hg1923073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983495
Samples
Known GenesC10orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452538
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