A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354345



Internal ID22141160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136278563..136278892hg38UCSC Ensembl
chrX:135360722..135361051hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3524971
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354345
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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