A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672026



Internal ID9938131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24859198..24860305hg38UCSC Ensembl
OuterchrX:24859041..24860458hg38UCSC Ensembl
InnerchrX:24877315..24878422hg19UCSC Ensembl
OuterchrX:24877158..24878575hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6495762
SamplesHG00336
Known GenesPOLA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672026
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