A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757586



Internal ID18731832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44690255..44694614hg38UCSC Ensembl
OuterchrX:44690007..44694771hg38UCSC Ensembl
InnerchrX:44549501..44553860hg19UCSC Ensembl
OuterchrX:44549253..44554017hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg384765
hg194765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757586
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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