A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757618



Internal ID18731864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:49640612..49654512hg38UCSC Ensembl
OuterchrX:49639888..49655482hg38UCSC Ensembl
InnerchrX:49405215..49419115hg19UCSC Ensembl
OuterchrX:49404491..49420085hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3815595
hg1915595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757618
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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