A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098434



Internal ID21492872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51079769..51079769hg38UCSC Ensembl
chr12:51473552..51473552hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661679
Supporting Variants
SamplesNA19238
Known GenesCSRNP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098434
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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