A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757984



Internal ID18732230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118278319..118278486hg38UCSC Ensembl
OuterchrX:118278286..118278488hg38UCSC Ensembl
InnerchrX:117412282..117412449hg19UCSC Ensembl
OuterchrX:117412249..117412451hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757984
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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