A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757777



Internal ID18732023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:82727228..82732546hg38UCSC Ensembl
OuterchrX:82726052..82733429hg38UCSC Ensembl
InnerchrX:81982677..81987995hg19UCSC Ensembl
OuterchrX:81981501..81988878hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg387378
hg197378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757777
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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