A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385103



Internal ID22314675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55930791..55930847hg38UCSC Ensembl
chrX:55957224..55957280hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV line1 deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231117
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsAbsence of a L1P mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385103
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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