A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258266



Internal ID21398047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16210630..18436487hg38UCSC Ensembl
chr16:16304487..18527500hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382225858
hg192223014
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730208
Supporting Variants
SamplesHG00512
Known GenesABCC6, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NOMO3, NPIPA7, NPIPA8, PKD1P1, XYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258266
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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