A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565267



Internal ID7036649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21583121..22701180hg38UCSC Ensembl
Outerchr16:21594442..22712501hg19UCSC Ensembl
Outerchr16:21501943..22620002hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381118060
hg191118060
hg181118060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998989
Supporting Variants
SamplesHuRef
Known GenesC16orf52, CDR2, EEF2K, IGSF6, LOC100190986, LOC653786, METTL9, NPIPB5, OTOA, PDZD9, POLR3E, RRN3P1, RRN3P3, SMG1P1, UQCRC2, VWA3A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565267
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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