A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454112



Internal ID22248749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2896970..2897368hg38UCSC Ensembl
chrX:2815011..2815409hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3185767
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)nssv14454112
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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