A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760197



Internal ID18734443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9318566..9327132hg38UCSC Ensembl
Outerchr3:9318082..9327456hg38UCSC Ensembl
Innerchr3:9360250..9368816hg19UCSC Ensembl
Outerchr3:9359766..9369140hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg389375
hg199375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760197
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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