A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282206



Internal ID20491424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97014975..97014975hg38UCSC Ensembl
chr15:97558205..97558205hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282206
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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