A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086301



Internal ID21487547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:34199306..34199306hg38UCSC Ensembl
chr12:34352241..34352241hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661829
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086301
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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