A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509988



Internal ID20883301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98086312..98100229hg38UCSC Ensembl
chr15:98629541..98643458hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3813918
hg1913918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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