A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286817



Internal ID20496035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13501505..13501505hg38UCSC Ensembl
chr1:13827955..13827955hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762245
Supporting Variants
Samples
Known GenesLRRC38
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286817
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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