A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757911



Internal ID18385471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:104157745..104158346hg38UCSC Ensembl
OuterchrX:104157733..104158364hg38UCSC Ensembl
InnerchrX:103402426..103403027hg19UCSC Ensembl
OuterchrX:103402414..103403045hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757911
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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