A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746404



Internal ID20522417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9786343..9796403hg38UCSC Ensembl
chr1:9846401..9856461hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3810061
hg1910061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292609
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746404
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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