A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096060



Internal ID22005293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1929983..1929983hg38UCSC Ensembl
chr12:2039149..2039149hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598382
Samples
Known GenesLINC00940
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096060
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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