A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387834



Internal ID22292758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153481272..153481324hg38UCSC Ensembl
chrX:152746730..152746782hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174021
Supporting Variants
SamplesNA19240
Known GenesHAUS7
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387834
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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