A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5726867



Internal ID9391410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62897257..62918220hg38UCSC Ensembl
OuterchrX:62897100..62918373hg38UCSC Ensembl
InnerchrX:62116727..62137690hg19UCSC Ensembl
OuterchrX:62116570..62137843hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3821274
hg1921274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661267
Supporting Variants
SamplesNA18595
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5726867
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