A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838356



Internal ID22613291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152676429..152729940hg38UCSC Ensembl
chr4:153597581..153651092hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3853512
hg1953512
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499700
Samples
Known GenesTMEM154
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838356
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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