A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558707



Internal ID18759783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24274597..24274895hg38UCSC Ensembl
OuterchrX:24274541..24274963hg38UCSC Ensembl
InnerchrX:24292714..24293012hg19UCSC Ensembl
OuterchrX:24292658..24293080hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757454
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558707
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