A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559034



Internal ID18760110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:82944260..82953279hg38UCSC Ensembl
OuterchrX:82943161..82953418hg38UCSC Ensembl
InnerchrX:82199268..82208287hg19UCSC Ensembl
OuterchrX:82198169..82208426hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3810258
hg1910258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757781
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559034
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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