A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039209



Internal ID20606249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81834007..81834953hg38UCSC Ensembl
chr17:79791883..79792829hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527482
Supporting Variants
Samples
Known GenesPPP1R27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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