A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760027



Internal ID20535887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148178719..148178719hg38UCSC Ensembl
chr6:148499855..148499855hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760027
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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