A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334052



Internal ID20867233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23856957..23860680hg38UCSC Ensembl
chr1:24183447..24187170hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383724
hg193724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202508
Samples
Known GenesFUCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334052
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