A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177394



Internal ID22334401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42239141..42239355hg38UCSC Ensembl
chrX:42098394..42098608hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463782
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)nsv3177394
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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