A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088943



Internal ID21998176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96101122..96101122hg38UCSC Ensembl
chr12:96494900..96494900hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088943
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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