A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210156



Internal ID22358119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54065193..54065701hg38UCSC Ensembl
chrX:54091626..54092134hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10129n152
Supporting Variantsnssv14391344
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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