A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325575



Internal ID20858706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:191278223..191459350hg38UCSC Ensembl
chr1:191247353..191428480hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38181128
hg19181128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481n223
Supporting Variantsnssv18199812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325575
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