A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757528



Internal ID18731774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33820884..33824883hg38UCSC Ensembl
OuterchrX:33819884..33825598hg38UCSC Ensembl
InnerchrX:33839001..33843000hg19UCSC Ensembl
OuterchrX:33838001..33843715hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg385715
hg195715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757528
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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