A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649439



Internal ID21597744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7660375..7660375hg38UCSC Ensembl
chr12:7812971..7812971hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085203
SamplesHG02587
Known GenesAPOBEC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649439
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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