A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558821



Internal ID18759897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:42653040..42654614hg38UCSC Ensembl
OuterchrX:42652729..42654620hg38UCSC Ensembl
InnerchrX:42512292..42513866hg19UCSC Ensembl
OuterchrX:42511981..42513872hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381892
hg191892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757568
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558821
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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