A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752958



Internal ID21391785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64364756..64366038hg38UCSC Ensembl
chr11:64132228..64133510hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431563
Supporting Variants
SamplesSMI018
Known GenesRPS6KA4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752958
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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