A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5714285



Internal ID9309480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16454054..16461127hg38UCSC Ensembl
chrX:16472177..16479250hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg387074
hg197074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666836
Supporting Variants
SamplesNA18499
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5714285
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