A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757616



Internal ID18731862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:49132167..49135157hg38UCSC Ensembl
OuterchrX:49132158..49135541hg38UCSC Ensembl
InnerchrX:48988501..48991500hg19UCSC Ensembl
OuterchrX:48988492..48991884hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383384
hg193393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757616
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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