A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224342



Internal ID20791382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127859627..127883312hg38UCSC Ensembl
chr9:130621906..130645591hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3823686
hg1923686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447686
Supporting Variants
Samples
Known GenesAK1, MIR4672
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224342
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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