A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178602



Internal ID22335091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112851758..112851877hg38UCSC Ensembl
chrX:112094986..112095105hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455085
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)nsv3178602
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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