A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191355



Internal ID20758396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72914062..72947068hg38UCSC Ensembl
chr17:70910201..70943207hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3833007
hg1933007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527020
Supporting Variants
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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