A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176335



Internal ID22333818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111879898..111880084hg38UCSC Ensembl
chrX:111123126..111123312hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14465022
SamplesHG00733
Known GenesTRPC5, TRPC5OS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176335
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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