A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757992



Internal ID18385552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119283917..119307320hg38UCSC Ensembl
OuterchrX:119282038..119307537hg38UCSC Ensembl
InnerchrX:118417880..118441283hg19UCSC Ensembl
OuterchrX:118416001..118441500hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3825500
hg1925500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757992
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