A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174764



Internal ID22332996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135012913..135012970hg38UCSC Ensembl
chrX:134146943..134147000hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10296n152
Supporting Variantsnssv14452675
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)nsv3174764
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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