A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429062



Internal ID22170597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9407127..9433352hg38UCSC Ensembl
chrX:9375167..9401392hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3826226
hg1926226
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186466
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429062
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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