A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757853



Internal ID18732099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94146200..94149716hg38UCSC Ensembl
OuterchrX:94145894..94149796hg38UCSC Ensembl
InnerchrX:93401199..93404715hg19UCSC Ensembl
OuterchrX:93400893..93404795hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383903
hg193903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757853
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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