A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177112



Internal ID22334250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38163989..38164725hg38UCSC Ensembl
chrX:38023242..38023978hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460711
SamplesHG00733
Known GenesSRPX
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177112
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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