A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187401



Internal ID20754441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24245120..24558369hg38UCSC Ensembl
chr15:24490267..24803516hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38313250
hg19313250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514570
Supporting Variants
Samples
Known GenesPWRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00582


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