A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651096



Internal ID21599401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30369659..30369659hg38UCSC Ensembl
chr12:30522592..30522592hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079409
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651096
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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