A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380968



Internal ID22286164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74212957..74213009hg38UCSC Ensembl
chrX:73432792..73432844hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183848
Supporting Variants
SamplesNA19240
Known GenesFTX
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380968
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