A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202996



Internal ID22352081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130150353..130150978hg38UCSC Ensembl
chrX:129284328..129284953hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353581, nssv14353582
SamplesNA19238, NA19239
Known GenesAIFM1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202996
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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