A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455217



Internal ID21112770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55096661..55362132hg38UCSC Ensembl
chr10:56856421..57121892hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38265472
hg19265472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv750n223
Supporting Variantsnssv17981938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455217
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