A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520992



Internal ID22390404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98301513..98429194hg38UCSC Ensembl
chrX:97556511..97684192hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38127682
hg19127682
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353104, nssv14353105, nssv14353106
SamplesNA19239, HG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3520992
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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