A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736200



Internal ID20512147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9923270..9923364hg38UCSC Ensembl
chr18:9923267..9923361hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259732
Samples
Known GenesVAPA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736200
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