A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257237



Internal ID21398314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14806736..15311665hg38UCSC Ensembl
chr16:14900593..15405522hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38504930
hg19504930
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730140
Supporting Variants
SamplesHG00513
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)nssv16257237
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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