A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219757



Internal ID20786797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74604074..74608491hg38UCSC Ensembl
chr7:74018400..74022817hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384418
hg194418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219757
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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