A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561518



Internal ID18762594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15803783..15804932hg38UCSC Ensembl
Outerchr3:15803574..15805257hg38UCSC Ensembl
Innerchr3:15845290..15846439hg19UCSC Ensembl
Outerchr3:15845081..15846764hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760265
Samples
Known GenesANKRD28
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561518
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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