A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222000



Internal ID20789040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120038480..120063871hg38UCSC Ensembl
chr7:119678534..119703925hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3825392
hg1925392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222000
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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