A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098674



Internal ID21492921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69461796..69461796hg38UCSC Ensembl
chr12:69855576..69855576hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645232
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098674
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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