A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198898



Internal ID22348566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28398503..28398909hg38UCSC Ensembl
chrX:28416620..28417026hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350759
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198898
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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