A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837487



Internal ID22612422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99605721..99611715hg38UCSC Ensembl
chr3:99324565..99330559hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg385995
hg195995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497544
Samples
Known GenesMIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837487
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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