A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663125



Internal ID21611430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103768604..103768604hg38UCSC Ensembl
chr12:104162382..104162382hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076543
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663125
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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