A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757471



Internal ID18731717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26675223..26702812hg38UCSC Ensembl
OuterchrX:26669884..26704780hg38UCSC Ensembl
InnerchrX:26693340..26720929hg19UCSC Ensembl
OuterchrX:26688001..26722897hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3834897
hg1934897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757471
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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