A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524889



Internal ID22391376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20094505..20094569hg38UCSC Ensembl
chrX:20112623..20112687hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10046n152
Supporting Variantsnssv14349999, nssv14350001, nssv14350000
SamplesNA19239, HG00732, HG00733
Known GenesMAP7D2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524889
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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