A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330456



Internal ID20863613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234857001..234868100hg38UCSC Ensembl
chr1:234992748..235003847hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3811100
hg1911100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330456
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