A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559471



Internal ID18760547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151442834..151532323hg38UCSC Ensembl
OuterchrX:151442029..151533110hg38UCSC Ensembl
InnerchrX:150611306..150700795hg19UCSC Ensembl
OuterchrX:150610501..150701582hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3891082
hg1991082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758218
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559471
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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