A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191932



Internal ID20758972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66700601..66703200hg38UCSC Ensembl
chr15:66992939..66995538hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513795
Supporting Variants
Samples
Known GenesSMAD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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