A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760121



Internal ID18734367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3831538..3831845hg38UCSC Ensembl
Outerchr3:3831475..3831871hg38UCSC Ensembl
Innerchr3:3873222..3873529hg19UCSC Ensembl
Outerchr3:3873159..3873555hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561374
Supporting Variants
Samples
Known GenesLRRN1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760121
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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