A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439946



Internal ID22231478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233764..47233817hg38UCSC Ensembl
chrX:47093163..47093216hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182068
Supporting Variants
SamplesHG00733
Known GenesUSP11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14439946
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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