A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197258



Internal ID22347161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48638017..48676575hg38UCSC Ensembl
chrX:48496405..48534964hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3838559
hg1938560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10116n152
Supporting Variantsnssv14374519
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)nsv3197258
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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