A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753940



Internal ID21386902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326646..14327080hg38UCSC Ensembl
chr11:14348192..14348626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431466
Supporting Variants
SamplesMDQ025
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753940
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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