A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228456



Internal ID20795496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74618016..74621509hg38UCSC Ensembl
chr7:74032335..74035824hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383494
hg193490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228456
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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