A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565931



Internal ID22434640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101515356..101515356hg38UCSC Ensembl
chrX:100770343..100770343hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353138, nssv14353137, nssv14353136
SamplesNA19238, NA19239, NA19240
Known GenesARMCX4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565931
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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