A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231953



Internal ID20798993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130132742..130149007hg38UCSC Ensembl
chr9:132895021..132911286hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3816266
hg1916266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449086
Supporting Variants
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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