A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460445



Internal ID22212999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46497420..46497850hg38UCSC Ensembl
chrX:46356855..46357285hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177637
Supporting Variants
SamplesHG00733
Known GenesZNF674
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460445
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