A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837257



Internal ID22612192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98855499..98917853hg38UCSC Ensembl
chr3:98574343..98636697hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3862355
hg1962355
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492201
Samples
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837257
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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