A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179929



Internal ID20746969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35295101..35303000hg38UCSC Ensembl
chr15:35587302..35595201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497095
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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