A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258582



Internal ID21400437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18607041..18827456hg38UCSC Ensembl
chr17:18510354..18730769hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38220416
hg19220416
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730068
Supporting Variants
SamplesNA19239
Known GenesCCDC144B, FBXW10, FOXO3B, TBC1D28, TRIM16L, TVP23B, ZNF286B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258582
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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