A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988316



Internal ID20555356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14305176..14309362hg38UCSC Ensembl
chr11:14326722..14330908hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436607
Supporting Variants
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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