A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757578



Internal ID18731824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43753686..43753822hg38UCSC Ensembl
OuterchrX:43753682..43753828hg38UCSC Ensembl
InnerchrX:43612933..43613069hg19UCSC Ensembl
OuterchrX:43612929..43613075hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757578
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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