A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757468



Internal ID18731714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26276401..26280232hg38UCSC Ensembl
OuterchrX:26276354..26280383hg38UCSC Ensembl
InnerchrX:26294518..26298349hg19UCSC Ensembl
OuterchrX:26294471..26298500hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg384030
hg194030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757468
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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