A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334168



Internal ID20867350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58320264..58437656hg38UCSC Ensembl
chr1:58785936..58903328hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38117393
hg19117393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334168
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