A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754155



Internal ID20530015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92603470..92603470hg38UCSC Ensembl
chr1:93069027..93069027hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270906
Samples
Known GenesEVI5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754155
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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