A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231656



Internal ID20798696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25675701..25682200hg38UCSC Ensembl
chr9:25675699..25682198hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429039
Supporting Variants
Samples
Known GenesTUSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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