A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265137



Internal ID20474355
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 StatusS
Merged Variantsnsv4752301
Supporting Variants
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265137
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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