A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757427



Internal ID18731673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:21782645..21782797hg38UCSC Ensembl
OuterchrX:21782639..21782804hg38UCSC Ensembl
InnerchrX:21800763..21800915hg19UCSC Ensembl
OuterchrX:21800757..21800922hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757427
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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