A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326642



Internal ID20859779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169404744..169411880hg38UCSC Ensembl
chr1:169373982..169381118hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg387137
hg197137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053678
Samples
Known GenesCCDC181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer