A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175668



Internal ID22333486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145990558..145991517hg38UCSC Ensembl
chrX:145072076..145073035hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10341n152
Supporting Variantsnssv14460887
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)nsv3175668
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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