A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235490



Internal ID20802530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39599101..39633700hg38UCSC Ensembl
chr7:39638700..39673299hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3834600
hg1934600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617283
Supporting Variants
Samples
Known GenesRALA, YAE1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00069


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