A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730532



Internal ID20506444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9774424..9782868hg38UCSC Ensembl
chr1:9834482..9842926hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg388445
hg198445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286526
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730532
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