A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748286



Internal ID21389499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:980114..980624hg38UCSC Ensembl
chr11:980114..980624hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431614
Supporting Variants
SamplesNB09
Known GenesAP2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748286
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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