A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178585



Internal ID22335077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730198..9730368hg38UCSC Ensembl
chrX:9698238..9698408hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10029n152
Supporting Variantsnssv14413371
SamplesHG00514
Known GenesGPR143
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178585
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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