A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228021



Internal ID20795061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38402197..38409698hg38UCSC Ensembl
chr9:38402194..38409695hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg387502
hg197502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441602
Supporting Variants
Samples
Known GenesIGFBPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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