A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753136



Internal ID20528996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188361517..188361517hg38UCSC Ensembl
chr3:188079305..188079305hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272385
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753136
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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