A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196239



Internal ID20763279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57444585..57444983hg38UCSC Ensembl
chr17:55521946..55522344hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533844
Supporting Variants
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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