A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757321



Internal ID18731567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5563960..5578062hg38UCSC Ensembl
OuterchrX:5562460..5578601hg38UCSC Ensembl
InnerchrX:5482001..5496103hg19UCSC Ensembl
OuterchrX:5480501..5496642hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3816142
hg1916142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757321
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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