A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751625



Internal ID20527485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149169080..149169080hg38UCSC Ensembl
chr5:148548643..148548643hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285568
Samples
Known GenesABLIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751625
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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