A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334192



Internal ID20867375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226253156..226254804hg38UCSC Ensembl
chr1:226440857..226442505hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381649
hg191649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058408
Samples
Known GenesLIN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334192
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