A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323018



Internal ID20856133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229840434..229912975hg38UCSC Ensembl
chr1:229976181..230048722hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3872542
hg1972542
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323018
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