A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257343



Internal ID21400476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21547957..22698517hg38UCSC Ensembl
chr16:21559278..22709838hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381150561
hg191150561
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)nssv16257343
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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