A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199599



Internal ID22349162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56073004..56073749hg38UCSC Ensembl
chrX:56099437..56100182hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351807
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199599
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