A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180610



Internal ID20747650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58885310..58888611hg38UCSC Ensembl
chr17:56962671..56965972hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530627
Supporting Variants
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180610
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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