A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10103n152



Internal ID22825806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45434811..45434873hg38UCSC Ensembl
chrX:45294056..45294118hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV line1 deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3234518, nsv3233395
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10103n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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