A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290139



Internal ID20499357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26842756..26842756hg38UCSC Ensembl
chr15:27087903..27087903hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768270
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290139
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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