A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210286



Internal ID22358230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:58539767..58555579hg38UCSC Ensembl
chrX:58566200..58582012hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3815813
hg1915813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351869, nssv14351870
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210286
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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