A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757627



Internal ID18731873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:52336256..52340861hg38UCSC Ensembl
OuterchrX:52336251..52340929hg38UCSC Ensembl
InnerchrX:52079398..52084003hg19UCSC Ensembl
OuterchrX:52079393..52084071hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg384679
hg194679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558880
Supporting Variants
Samples
Known GenesMIR8088
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757627
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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