A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761761



Internal ID18736007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184585786..184587472hg38UCSC Ensembl
Outerchr3:184585776..184587481hg38UCSC Ensembl
Innerchr3:184303574..184305260hg19UCSC Ensembl
Outerchr3:184303564..184305269hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761761
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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