A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565834



Internal ID22434543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39247290..39247290hg38UCSC Ensembl
chrX:39106543..39106543hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350286, nssv14350287, nssv14350285
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565834
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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