A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922579



Internal ID22697804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25989650..25989766hg38UCSC Ensembl
chr12:26142583..26142699hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363677
Samples
Known GenesRASSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922579
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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