A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318044



Internal ID20851135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114482645..114483190hg38UCSC Ensembl
chr1:115025267..115025812hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051647
Samples
Known GenesTRIM33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318044
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