A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354860



Internal ID22282775
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196398
Supporting Variants
SamplesNA19239
Known GenesGABRA3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354860
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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