A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285568



Internal ID20494786
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 StatusS
Merged Variantsnsv4751625
Supporting Variants
Samples
Known GenesABLIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285568
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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