A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758042



Internal ID20533902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37774863..37774863hg38UCSC Ensembl
chr6:37742639..37742639hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758042
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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