A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256111



Internal ID21400444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14815740..15327066hg38UCSC Ensembl
chr16:14909597..15420923hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38511327
hg19511327
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730140
Supporting Variants
SamplesNA19239
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, NTAN1, PDXDC1, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256111
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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