A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558498



Internal ID18759574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1611592..1611956hg38UCSC Ensembl
OuterchrX:1611569..1611974hg38UCSC Ensembl
InnerchrX:1730485..1730849hg19UCSC Ensembl
OuterchrX:1730462..1730867hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757245
Samples
Known GenesASMT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558498
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