A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258132



Internal ID21400312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21567330..22701560hg38UCSC Ensembl
chr16:21578651..22712881hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381134231
hg191134231
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730273
Supporting Variants
SamplesNA19239
Known GenesC16orf52, CDR2, EEF2K, IGSF6, LOC653786, METTL9, NPIPB5, OTOA, PDZD9, POLR3E, RRN3P1, RRN3P3, SMG1P1, UQCRC2, VWA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258132
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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