A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757667



Internal ID18731913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:64763121..64772970hg38UCSC Ensembl
OuterchrX:64762957..64773120hg38UCSC Ensembl
InnerchrX:63983001..63992850hg19UCSC Ensembl
OuterchrX:63982837..63993000hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3810164
hg1910164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757667
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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