A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757834



Internal ID18732080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:90194475..90241583hg38UCSC Ensembl
OuterchrX:90193502..90243811hg38UCSC Ensembl
InnerchrX:89449474..89496582hg19UCSC Ensembl
OuterchrX:89448501..89498810hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3850310
hg1950310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757834
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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