A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189765



Internal ID20756805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58880692..58942648hg38UCSC Ensembl
chr17:56958053..57020009hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3861957
hg1961957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530845
Supporting Variants
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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