A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731219



Internal ID20507137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19467360..19467437hg38UCSC Ensembl
chr1:19793854..19793931hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285807
Samples
Known GenesCAPZB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731219
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