A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190291



Internal ID22341200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145990558..145991524hg38UCSC Ensembl
chrX:145072076..145073042hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10341n152
Supporting Variantsnssv14404055
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190291
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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