A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757604



Internal ID18385164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:47506780..47521860hg38UCSC Ensembl
OuterchrX:47505404..47522364hg38UCSC Ensembl
InnerchrX:47366179..47381259hg19UCSC Ensembl
OuterchrX:47364803..47381763hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3816961
hg1916961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757604
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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