A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10341n152



Internal ID22826044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145990558..145991524hg38UCSC Ensembl
chrX:145072076..145073042hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3190291, nsv3175668
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)dgv10341n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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