A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5883303



Internal ID9568499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4464139..4473987hg38UCSC Ensembl
chrX:4382180..4392028hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg389849
hg199849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674973
Supporting Variants
SamplesNA19116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5883303
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer