A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902204



Internal ID22677360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136844541..136846902hg38UCSC Ensembl
chr3:136563383..136565744hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390706
Samples
Known GenesSLC35G2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902204
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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