A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757467



Internal ID18731713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26266400..26268270hg38UCSC Ensembl
OuterchrX:26266374..26268343hg38UCSC Ensembl
InnerchrX:26284517..26286387hg19UCSC Ensembl
OuterchrX:26284491..26286460hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381970
hg191970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757467
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