A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748150



Internal ID21391691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90671633..90672295hg38UCSC Ensembl
chr12:91065410..91066072hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431849
Supporting Variants
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748150
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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