A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754491



Internal ID20530351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141691107..141691107hg38UCSC Ensembl
chr4:142612260..142612260hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287980
Samples
Known GenesIL15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754491
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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