A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757296



Internal ID18384856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:3287016..3298459hg38UCSC Ensembl
OuterchrX:3286960..3298959hg38UCSC Ensembl
InnerchrX:3205057..3216500hg19UCSC Ensembl
OuterchrX:3205001..3217000hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757296
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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