A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226331



Internal ID20793371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17051182..17566670hg38UCSC Ensembl
chr7:17090806..17606294hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38515489
hg19515489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616896
Supporting Variants
Samples
Known GenesAHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226331
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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