A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757568



Internal ID18731814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:42653040..42654614hg38UCSC Ensembl
OuterchrX:42652729..42654620hg38UCSC Ensembl
InnerchrX:42512292..42513866hg19UCSC Ensembl
OuterchrX:42511981..42513872hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381892
hg191892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558821
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757568
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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