A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221785



Internal ID20788825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129428101..129442100hg38UCSC Ensembl
chr9:132190380..132204379hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.4039


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