A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225906



Internal ID20792946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34717355..34825102hg38UCSC Ensembl
chr9:34717352..34825099hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38107748
hg19107748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441870
Supporting Variants
Samples
Known GenesFAM205A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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