A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238126



Internal ID22374067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84859391..84870914hg38UCSC Ensembl
chrX:84114398..84125920hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3811524
hg1911523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352470, nssv14352471
SamplesNA19239, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238126
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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