A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559187



Internal ID18760263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112615040..112615140hg38UCSC Ensembl
OuterchrX:112615032..112615145hg38UCSC Ensembl
InnerchrX:111858268..111858368hg19UCSC Ensembl
OuterchrX:111858260..111858373hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757934
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559187
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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