A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230086



Internal ID20797126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46429220..46448574hg38UCSC Ensembl
chr7:46468818..46488172hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3819355
hg1919355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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