A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350985



Internal ID22231019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3483706..3483823hg38UCSC Ensembl
chrX:3401747..3401864hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210129
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350985
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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