A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092934



Internal ID21462197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92071727..92072044hg38UCSC Ensembl
chr12:92465503..92465820hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602536
Supporting Variants
SamplesHG02818
Known GenesC12orf79
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092934
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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