A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172919



Internal ID22332052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51083053..51083272hg38UCSC Ensembl
chrX:50825899..50826118hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412981
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3172919
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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