A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834533



Internal ID22609468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111592259..111594277hg38UCSC Ensembl
chr3:111311106..111313124hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382019
hg192019
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483766
Samples
Known GenesCD96, ZBED2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834533
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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