A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836092



Internal ID22611027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58958658..58978852hg38UCSC Ensembl
chr3:58944384..58964578hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3820195
hg1920195
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493895
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836092
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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