A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256805



Internal ID21400664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18607812..18875217hg38UCSC Ensembl
chr17:18511125..18778530hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38267406
hg19267406
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730068
Supporting Variants
SamplesNA19240
Known GenesCCDC144B, FBXW10, FOXO3B, PRPSAP2, TBC1D28, TRIM16L, TVP23B, ZNF286B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256805
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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