A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928904



Internal ID22704150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13127465..13128162hg38UCSC Ensembl
chr18:13127464..13128161hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928904
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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