A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330028



Internal ID20863182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64810994..64812604hg38UCSC Ensembl
chr1:65276677..65278287hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381611
hg191611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204289
Samples
Known GenesRAVER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330028
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