A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752301



Internal ID20528161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38507954..38507954hg38UCSC Ensembl
chr21:39879878..39879878hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265137
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752301
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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