A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565755



Internal ID22434469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12924466..12924466hg38UCSC Ensembl
chrX:12942585..12942585hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349896, nssv14349895
SamplesNA19238, NA19240
Known GenesTLR8-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565755
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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