A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191507



Internal ID20758547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78111878..78112444hg38UCSC Ensembl
chr17:76107959..76108525hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520678
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191507
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00029


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