A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984827



Internal ID20551868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87868599..87868975hg38UCSC Ensembl
chr10:89628356..89628732hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438371
Supporting Variants
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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