A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364836



Internal ID21022389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9857340..9863852hg38UCSC Ensembl
chr3:9899024..9905536hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg386513
hg196513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364836
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