A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754178



Internal ID20530038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:313085..313085hg38UCSC Ensembl
chr19:313085..313085hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273103
Samples
Known GenesMIER2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754178
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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