A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323889



Internal ID20857012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236285137..236285637hg38UCSC Ensembl
chr1:236448437..236448937hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323889
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