A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705035



Internal ID21377311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10805657..10805747hg38UCSC Ensembl
chr11:10827204..10827294hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389680
Supporting Variants
Samples
Known GenesEIF4G2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705035
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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