A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757659



Internal ID18731905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62769224..62780623hg38UCSC Ensembl
OuterchrX:62768337..62780702hg38UCSC Ensembl
InnerchrX:61988694..62000093hg19UCSC Ensembl
OuterchrX:61987807..62000172hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3812366
hg1912366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757659
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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