A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757674



Internal ID18731920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:65801210..65824307hg38UCSC Ensembl
OuterchrX:65801132..65824658hg38UCSC Ensembl
InnerchrX:65021052..65044149hg19UCSC Ensembl
OuterchrX:65020974..65044500hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3823527
hg1923527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757674
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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