A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196147



Internal ID22346211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107622944..107622995hg38UCSC Ensembl
chrX:106866174..106866225hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353859
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196147
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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