A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333226



Internal ID20866402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47604224..47615739hg38UCSC Ensembl
chr1:48069896..48081411hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3811516
hg1911516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333226
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