A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757333



Internal ID20533193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57350841..57350841hg38UCSC Ensembl
chr20:55925897..55925897hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264111
Samples
Known GenesMIR5095
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757333
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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