A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938802



Internal ID22714188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27044291..27044573hg38UCSC Ensembl
chr18:24624255..24624537hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388022
Samples
Known GenesCHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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