A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757398



Internal ID18731644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:16579330..16584167hg38UCSC Ensembl
OuterchrX:16578378..16584377hg38UCSC Ensembl
InnerchrX:16597453..16602290hg19UCSC Ensembl
OuterchrX:16596501..16602500hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757398
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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