A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758266



Internal ID18385826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155560527..155560768hg38UCSC Ensembl
OuterchrX:155560499..155560800hg38UCSC Ensembl
InnerchrX:154790188..154790429hg19UCSC Ensembl
OuterchrX:154790160..154790461hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559519
Supporting Variants
Samples
Known GenesTMLHE
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758266
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