A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565849



Internal ID22434558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75708863..75708863hg38UCSC Ensembl
chrX:74928698..74928698hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352250, nssv14352247, nssv14352248, nssv14352246, nssv14352245, nssv14352249
SamplesHG00512, NA19238, NA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565849
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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