A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660047



Internal ID21608352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53803192..53803192hg38UCSC Ensembl
chr12:54196976..54196976hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083250
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660047
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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