A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559314



Internal ID18760390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128258024..128293844hg38UCSC Ensembl
OuterchrX:128257857..128294022hg38UCSC Ensembl
InnerchrX:127392001..127427822hg19UCSC Ensembl
OuterchrX:127391834..127428000hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3836166
hg1936167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758061
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559314
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