A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321629



Internal ID20854737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165628301..165633800hg38UCSC Ensembl
chr1:165597538..165603037hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201939
Samples
Known GenesMGST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321629
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