A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107339



Internal ID22016572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14689409..15363653hg38UCSC Ensembl
chr16:14783266..15457510hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38674245
hg19674245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607356
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, NPIPA5, NTAN1, PDXDC1, PLA2G10, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107339
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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