A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761122



Internal ID18388682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111073934..111077456hg38UCSC Ensembl
Outerchr3:111073879..111077587hg38UCSC Ensembl
Innerchr3:110792781..110796303hg19UCSC Ensembl
Outerchr3:110792726..110796434hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383709
hg193709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562375
Supporting Variants
Samples
Known GenesPVRL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761122
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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