A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182136



Internal ID20749176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97985990..97987970hg38UCSC Ensembl
chr15:98529220..98531200hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00033


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