A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440420



Internal ID21097973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53215460..53340281hg38UCSC Ensembl
chr10:54975220..55100041hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38124822
hg19124822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440420
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