A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525319



Internal ID22394696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79469358..79469413hg38UCSC Ensembl
chrX:78724855..78724910hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352346, nssv14352348, nssv14352347, nssv14352345
SamplesNA19238, HG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525319
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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