A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558783



Internal ID18759859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34025223..34054383hg38UCSC Ensembl
OuterchrX:34023384..34060496hg38UCSC Ensembl
InnerchrX:34043340..34072500hg19UCSC Ensembl
OuterchrX:34041501..34078613hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3837113
hg1937113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757530
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558783
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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