A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834818



Internal ID22609753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183716201..183717200hg38UCSC Ensembl
chr3:183433989..183434988hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490035
Samples
Known GenesYEATS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834818
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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