A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795222



Internal ID21240560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75204690..75223663hg38UCSC Ensembl
chr16:75238588..75257561hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818974
hg1918974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705592
SamplesCHM1
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795222
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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