A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179968



Internal ID20747008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45028401..45032100hg38UCSC Ensembl
chr15:45320599..45324298hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514519
Supporting Variants
Samples
Known GenesSORD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.16846


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