A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833911



Internal ID22608846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105489094..105495620hg38UCSC Ensembl
chr3:105207938..105214464hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg386527
hg196527
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1506n209
Supporting Variantsnssv17489151
Samples
Known GenesALCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833911
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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