A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834329



Internal ID22609264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137989496..138007771hg38UCSC Ensembl
chr3:137708338..137726613hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3818276
hg1918276
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485141
Samples
Known GenesCLDN18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834329
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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