A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353139



Internal ID22280872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101662146..101662484hg38UCSC Ensembl
chrX:100917131..100917469hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194545
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353139
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer