A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656141



Internal ID21604446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43791220..43791220hg38UCSC Ensembl
chr12:44185023..44185023hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090947
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656141
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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