A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758851



Internal ID20534711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:899518..899518hg38UCSC Ensembl
chr5:899633..899633hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290182
Samples
Known GenesTRIP13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758851
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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