A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656302



Internal ID21604607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47360962..47360962hg38UCSC Ensembl
chr12:47754745..47754745hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089276
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656302
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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