A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757250



Internal ID18731496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1637433..1641248hg38UCSC Ensembl
OuterchrX:1636892..1641607hg38UCSC Ensembl
InnerchrX:1756326..1760141hg19UCSC Ensembl
OuterchrX:1755785..1760500hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg384716
hg194716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558503
Supporting Variants
Samples
Known GenesASMT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757250
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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