A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558582



Internal ID18759658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6100460..6109218hg38UCSC Ensembl
OuterchrX:6098754..6109459hg38UCSC Ensembl
InnerchrX:6018501..6027259hg19UCSC Ensembl
OuterchrX:6016795..6027500hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3810706
hg1910706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757329
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558582
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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