A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352471



Internal ID22280129
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238126
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352471
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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