A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188992



Internal ID22340540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136033603..136033661hg38UCSC Ensembl
chrX:135115762..135115820hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438679
SamplesHG00733
Known GenesSLC9A6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188992
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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