A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839523



Internal ID22614458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26775015..26909518hg38UCSC Ensembl
chr4:26776637..26911140hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38134504
hg19134504
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493411
Samples
Known GenesSTIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839523
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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