A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187955



Internal ID20754995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45391474..45398301hg38UCSC Ensembl
chr15:45683672..45690499hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg386828
hg196828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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