A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322489



Internal ID20855602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187385681..187437965hg38UCSC Ensembl
chr1:187354813..187407097hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3852285
hg1952285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322489
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