A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834518



Internal ID22609453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111556121..111616556hg38UCSC Ensembl
chr3:111274968..111335403hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3860436
hg1960436
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489198
Samples
Known GenesCD96, ZBED2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834518
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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