A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452675



Internal ID22247551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135012913..135012970hg38UCSC Ensembl
chrX:134146943..134147000hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174764
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)nssv14452675
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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