A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455125



Internal ID22249602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78202724..78203750hg38UCSC Ensembl
chrX:77458221..77459247hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174146
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455125
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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