A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177909



Internal ID22334694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136185122..136185309hg38UCSC Ensembl
chrX:135267281..135267468hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462587
SamplesHG00733
Known GenesFHL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177909
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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