A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757583



Internal ID18731829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44520600..44522100hg38UCSC Ensembl
OuterchrX:44520541..44522251hg38UCSC Ensembl
InnerchrX:44379846..44381346hg19UCSC Ensembl
OuterchrX:44379787..44381497hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757583
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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