A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654138



Internal ID21602443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95010125..95010125hg38UCSC Ensembl
chr12:95403901..95403901hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081021
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654138
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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