A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432697



Internal ID21394699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58003794..58004127hg38UCSC Ensembl
chr18:55671026..55671359hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750030
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432697
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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