A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753104



Internal ID20528964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98289086..98289086hg38UCSC Ensembl
chr8:99301314..99301314hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294164
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753104
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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