A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332114



Internal ID20865283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16220313..16227054hg38UCSC Ensembl
chr1:16546808..16553549hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg386742
hg196742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332114
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