A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196398



Internal ID22346413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152361086..152361572hg38UCSC Ensembl
chrX:151529558..151530044hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354860
SamplesNA19239
Known GenesGABRA3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196398
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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