A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757886



Internal ID18732132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98585345..98650577hg38UCSC Ensembl
OuterchrX:98585003..98654002hg38UCSC Ensembl
InnerchrX:97840343..97905575hg19UCSC Ensembl
OuterchrX:97840001..97909000hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3869000
hg1969000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559139
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757886
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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