A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178027



Internal ID20745067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68725963..68729639hg38UCSC Ensembl
chr17:66722104..66725780hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg383677
hg193677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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