A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558856



Internal ID18413246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:47469954..47476101hg38UCSC Ensembl
OuterchrX:47469102..47477101hg38UCSC Ensembl
InnerchrX:47329353..47335500hg19UCSC Ensembl
OuterchrX:47328501..47336500hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757603
Samples
Known GenesZNF41
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558856
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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