A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329775



Internal ID20862928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234632454..234637086hg38UCSC Ensembl
chr1:234768200..234772832hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg384633
hg194633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202392
Samples
Known GenesLINC00184
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329775
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer