A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227332



Internal ID20794372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46888304..46951819hg38UCSC Ensembl
chr7:46927902..46991417hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3863516
hg1963516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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